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Managing site staff, proactively identify and resolve issues, and work to ensure successful site operations.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOverseeing all payroll, absence tracking/approvals, new hire orientation, and training per operational needs.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCollaborating with investigators to ensure patient safety and meeting client goals and timelines.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEmploying strategic thinking and problem-solving skills to propose and implement risk mitigations.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eParticipating and presenting in management or site meetings.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform all other duties as required or assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Kara Bardram","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A Bachelor’s degree AND 5+ years of clinical research experience or an equivalent combination of education and experience is required.\u0026nbsp; 2+ years of management experience required.\u0026nbsp; Clinical research site management experience required. \u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u003cbr\u003e\u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm).\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess strong organizational, time management, problem solving, and project management skills to meet project deadlines.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Site Director","url":"https://alcanzaclinical.pinpointhq.com/en/postings/8aecf075-cf2f-40f2-a599-f31bcc22f147","path":"/en/postings/8aecf075-cf2f-40f2-a599-f31bcc22f147","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"482599","requisition_id":"PIN-1471","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"11668","city":"Charlottesville ","name":"Charlottesville Medical Research Center | Charlottesville, VA","postal_code":"22911","province":"Virginia"}},{"id":"475626","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TX and Puerto Rico. 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Provides on-site oversight to help ensure execution and coordination of clinical research activities according to ICH guidelines, GCP, FDA guidelines and follows company policies and procedures.\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eOverall team management and leadership support with a focus on driving study performance, enhancing efficiencies, patient safety and protocol/GCP/regulatory compliance.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCollaborating with other departments (Business Development, Patient Recruitment, Finance, Budgets and Contracts, and Quality) to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eReviewing the performance dashboards and other clinical trial systems to oversee site and patient activities, ensure proper staff coverage, and to ensure the data has been updated to reflect timely execution of all operational aspects (required visits/calls, duration, and frequency).\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOverseeing resourcing allocations, site assignments and study team members' output and performance, to ensure study deliverables are on track, identifying risks to delivery or quality, and escalating any risks to clinical trial management deliverables (timeline, quality and budget).\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssisting with initial and ongoing trainings regarding protocol specificities, Case Report Form (CRF) completion, Standard Operating Procedures (SOPs), clinical plans and guidelines, and timelines for the study.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring adherence to standard operating procedures, good clinical practice (GCP), FDA regulations, and company policies and procedures.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOverseeing site staff assigned to the study and routinely assessing study-specific process and training compliance, CMP compliance, and identifies emerging risks. May develop and support execution of corrective action plans at site and study level.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOverseeing people management activities including timecards, absence tracking/approvals, new hire training, interviewing and selection, performance appraisals, job description preparation, employee counseling, career coaching and employment meetings.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eManaging assigned site staff, proactively identify and resolve issues, and work to ensure successful site operations.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCollaborating with investigators to ensure patient safety and meeting client goals and timelines.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEmploying strategic thinking and problem-solving skills to propose and implement risk mitigations.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eParticipating and presenting in management or site meetings.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform all other duties as required or assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Michelle Echeandia","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications:\u003c/strong\u003e\u003cbr\u003eBachelor’s degree and a minimum of 2 years of clinical research experience, or an equivalent combination of education and experience, is required. 2+ years’ experience as a clinical research coordinator (CRC). 1+ years of management experience in clinical research is highly preferred. Bi-lingual (English / Spanish) proficiency is a plus.\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eRequired Skills:\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm).\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess strong organizational, time management, problem solving, and project management skills to meet project deadlines.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Operations Manager - Bilingual required (English/Spanish)","url":"https://alcanzaclinical.pinpointhq.com/en/postings/90a9623a-401c-4646-b977-31b2ab11adf5","path":"/en/postings/90a9623a-401c-4646-b977-31b2ab11adf5","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"484806","requisition_id":"PIN-1476","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"32152","city":"San Juan","name":"FDI Clinical Research - San Juan","postal_code":"00927","province":"Puerto Rico"}},{"id":"483583","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eClinical Research Nurse \u003c/strong\u003eworks to ensure the execution of assigned studies, and performs clinical procedures, such as venipunctures, injections, prep or mixing of investigational study drugs and infusions, under the scope of the study protocol and in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties: \u003c/strong\u003eIn collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. 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blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming procedures commensurate with licensure including vitals, ECGs/EKGs, venipunctures, injections, infusions, mixing drug and/or dispense investigational product; etc.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRequesting and tracking medical record requests;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUpdating and maintaining logs, chart filings;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining \u0026amp; ordering study specific supplies;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eScheduling subjects for study visits and conducts appointment reminders;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eBuilding/updating source as needed;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eConducting monitoring visits and resolves issues as needed in a timely manner;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring study related reports and patient results are reviewed by investigator in a timely manner;\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Filing SAE/Deviation reports to Sponsor and IRB as needed;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Documenting and reporting adverse events;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Reporting non-compliance to appropriate staff in timely manner;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Maintaining positive and effective communication with clients and team members;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Always practicing ALCOAC principles with all documentation;\u003cbr\u003e\u0026nbsp;\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eBe thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePrepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay set up, train and maintain all technology needed for studies.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with study recruitment, patient enrollment, and tracking as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining confidentiality of patients, customers and company information, and;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming all other duties as requested or assigned.\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Adrianna Doggett","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A Bachelor’s degree in Nursing (BSN) AND a minimum of 1 year of clinical experience, OR an equivalent combination of education and experience, is required.\u0026nbsp; An active, unrestricted RN license, in state of work location, is required.\u0026nbsp; BLS certification required.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u0026nbsp; \u003cbr\u003e \u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with performing clinical procedures such as injections, vitals, EKGs, phlebotomy, infusions, etc. is required. \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStrong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks, and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Registered Nurse","url":"https://alcanzaclinical.pinpointhq.com/en/postings/a0957298-5df9-48b4-9cfc-941ec164e3b3","path":"/en/postings/a0957298-5df9-48b4-9cfc-941ec164e3b3","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"492014","requisition_id":"PIN-1505","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"11668","city":"Charlottesville ","name":"Charlottesville Medical Research Center | Charlottesville, VA","postal_code":"22911","province":"Virginia"}},{"id":"486853","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. \u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003ePrincipal Investigator \u003c/strong\u003econducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. 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Board certification in area of specialty is required. 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We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. \u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eLab Coordinator\u003c/strong\u003e works to ensure the execution of assigned lab procedures in compliance with GCP, ICH, FED and HIPAA regulations, company SOPs, and policies. \u0026nbsp;\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties: \u003c/strong\u003eResponsibilities may include but are not limited to:\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eDraw and process specimens according to each trial’s requirements\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssist with specimen shipments to central labs and ensure proper shipping methods have been observed\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor expiration dates on lab equipment and supplies\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUnpack and put away incoming lab supply shipments\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor and maintain both general and study-specific lab inventory, and ensure study-specific lab supplies are ready for new study start-up\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eTransport samples\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eProvide mentoring to new hires and allow them to shadow you as they learn.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete and renew CITI GCP and IATA training as required.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAttend SIVs when needed, and complete all sponsor-required lab training.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay support other clinical research-related activities such as recruitment, EDC and QA/Chart review as needed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring compliance with company SOPs, FDA/HIPAA regulations, ICF documentation, and GCP guidelines\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining confidentiality of patients, customers, and company information, and\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming other related activities as assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Andrew Rodriguez","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; High School diploma or equivalent and a minimum of 1 year of clinical laboratory processing experience is required. 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We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. \u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003ePrincipal Investigator \u003c/strong\u003econducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.\u003c/div\u003e","employment_type":"part_time","employment_type_text":"Part Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eEnsures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs \u0026amp; HIPAA guidelines, study protocols, as well as company policies and processes\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOverall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEvaluates and assesses participants to ensure only eligible participants enroll into the trials.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eParticipates and engages in successful delivery and retention of study participants.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eInteracts positively and collaboratively with sponsors, clients and team members.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePractices attention to detail in recording data and participant information, following protocol guidelines and GCPs.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eActively involved in protocol training for staff.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eParticipate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Michelle Echeandia","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications:\u003c/strong\u003e\u0026nbsp; MD or DO degree, an active physician license (in good standing) in the state of practice for this role. 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We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. 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Bi-lingual (English / Spanish) proficiency is highly preferred.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed listening skills and the ability to work well alone as well as in a team atmosphere. \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle multiple tasks and changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of honesty and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and help find solutions.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive patient health information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Patient Liaison (Patient Recruiter)","url":"https://alcanzaclinical.pinpointhq.com/en/postings/f0001de1-3027-4853-aca6-e9c023752c8b","path":"/en/postings/f0001de1-3027-4853-aca6-e9c023752c8b","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"507175","requisition_id":"PIN-1558","department":{"id":"21158","name":"Patient Recruitment "},"division":null,"structure_custom_group_one":null},"location":{"id":"11666","city":"Farmington","name":"Quest Research Institute - Farmington Hills, MI","postal_code":"48334","province":"Michigan"}},{"id":"500630","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eInvestigational Product Coordinator \u003c/strong\u003eis responsible for preparing and dispensing study drug, providing drug-related information to subjects and staff in compliance with GCP, ICH, HIPAA, FDA, USP 797, USP 800, state Boards of Pharmacy, and company SOPs. \u0026nbsp;\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eUnder the direction of the Lead Research Pharmacist (or similar) and the Principal/Sub Investigators, conducts the following according to study protocol, company processes \u0026amp; procedures, and in compliance with GCP, ICH, HIPPA, FDA, USP 797, USP 800, state Boards of Pharmacy and company SOPs:\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Integration of investigational medication use, pharmacy workflow, subject medication safety activities and regulatory standards;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Coordinating, and advising site staff on drug distribution services for investigational medications;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Identify and justify needs for additional resources, or redeploying resources in new ways to meet needs;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Prepares, labels (if required) and dispenses investigational medications, and provides drug-related information and education for subjects and site staff;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Dispenses controlled substances as part of a research study.\u0026nbsp; Maintains appropriate inventory records, documentation of receipt and ensures proper storage conditions\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsures safety and care for all research subjects as it relates to investigational medication preparation and dispensing;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePromotes individual professional growth and development by meeting requirements for mandatory/continuing education and skills competency; supports department-based goals which contribute to the success of the organization; serves as mentor and resource to less experienced staff\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOther duties as assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Omar Orama","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; An associate’s degree and 1+ years’ related experience, OR an equivalent combination of education and experience, is required. \u0026nbsp; Certified Pharmacy Technician (CPhT) credential is required.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is required.\u0026nbsp; \u003cbr\u003e\u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, web applications,\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStrong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, management, and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Certified Pharmacy Technician - Bilingual required (English/Spanish)","url":"https://alcanzaclinical.pinpointhq.com/en/postings/6f9ceae0-0d9d-4916-a598-99b91298023a","path":"/en/postings/6f9ceae0-0d9d-4916-a598-99b91298023a","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"507869","requisition_id":"PIN-1554","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"30854","city":"Palmetto Bay","name":"Innovation - Palmetto Bay, FL","postal_code":"","province":"Florida"}},{"id":"500832","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. \u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003ePatient Liaison\u003c/strong\u003e is responsible for supporting onsite patient recruitment efforts by\u003cbr\u003econducting pre-qualification, pre-screening, and scheduling activities to ensure a smooth and efficient enrollment process.\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eExecute onsite patient pre-screening and a focus on pivoting qualified patients into active studies for dedicated and local sites should patient be willing to travel.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEvaluate eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with site clinic staff. Support patient path to enrollment, managing all follow up and communication including reminder calls, rescheduling, etc.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor/manage onsite patient screening visit schedule – schedule/ reschedule appointments as needed or requested.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOwn No-Show/DNQ tracking, triaging, optimization.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCapture/manage inbound physician referral leads.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAddress and resolve patient barriers to study entry by leveraging knowledge of site or sponsor-provided support services, such as transportation assistance and reimbursement programs.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsure timely and consistent updating to Clinical Conductor/CTMS – updating patient touches/patient profile statuses, etc.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCreate targeted call lists based on i/e criteria in CTMS to best target patient populations for call efficiency.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePosition shares accountability for regional recruitment results. Drive screening numbers to meet recruitment goals set by leadership. Assist with collection of performance metrics related to attribution capability for screening visits.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eImmediately notify RSLs and/or recruitment leadership of any barriers and/or challenges to screens scheduled or completed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAcquire and continuously update knowledge of clinical research studies, including detailed understanding of their inclusion and exclusion criteria.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eManage patient portal leads (central campaigns) to include review, calling and updating patient leads.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor status of Refer-A-Friend campaigns\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRepresent company with HCP referral partners for local support and relationship management.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSupport planning and participate in local community outreach events to engage/educate patients about clinical trials, as needed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with new recruiter training and retraining of current team members.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform all other duties that may be requested or assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Caryn Gibson","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A high school diploma, or equivalent, AND a minimum of 5 years’ experience in a medical, healthcare, or medical research environment, or a similar field, or an equivalent combination of education and experience, is required.\u0026nbsp; Experience with therapy areas, customer service, calendar management /scheduling and CTMS (Clinical Trial Management System) experience is preferred.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eRequired Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as email, electronic health records, and basic applications.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to type proficiently (40+ wpm).\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess strong organizational skills, attention to detail, and have basic math proficiency.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is highly preferred.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed listening skills and the ability to work well alone as well as in a team atmosphere. \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle multiple tasks and changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of honesty and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and help find solutions.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive patient health information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Patient Liaison - ( Patient Recruitment )","url":"https://alcanzaclinical.pinpointhq.com/en/postings/621933c5-7238-437c-97c9-0306c3deabd1","path":"/en/postings/621933c5-7238-437c-97c9-0306c3deabd1","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"508069","requisition_id":"PIN-1565","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"11668","city":"Charlottesville ","name":"Charlottesville Medical Research Center | Charlottesville, VA","postal_code":"22911","province":"Virginia"}},{"id":"502486","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. 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Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eClinical Site Director \u003c/strong\u003eis responsible for driving operational performance for of the research site.\u0026nbsp; Provides on-site oversight to help ensure execution and coordination of clinical research activities according to ICH guidelines, GCP, and FDA guidelines and follows company policies and procedures.\u0026nbsp;\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eOverall site management and leadership with a focus on driving site performance, enhancing efficiencies, pati,ent safety and protocol/GCP/regulatory compliance.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCollaborating with department leaders in Business Development, Patient Recruitment, Finance, and Budgets Contracts and Quality to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eReviewing the performance dashboards and other clinical trial systems to oversee site and patient activities, ensure proper staff coverage, and to ensure the data has been updated to reflect timely execution of all operational aspects (required visits/calls, duration, and frequency).\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOverseeing resourcing allocations, site assignments and study team members' output and performance, to ensure study deliverables are on track, identifying risks to delivery or quality, and escalating any risks to clinical trial management deliverables (timeline, quality and budget).\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssisting with initial and ongoing trainings regarding protocol specificities, Case Report Form (CRF) completion, Standard Operating Procedures (SOPs), clinical plans and guidelines, and timelines for the study.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring adherence to standard operating procedures, good clinical practice (GCP), FDA regulations, and company policies and procedures.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOverseeing site staff assigned to the study and routinely assessing study-specific process and training compliance, CMP compliance, and identifies emerging risks.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDevelop and support execution of corrective action plans at site and study level.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOverseeing people management activities including interviewing and selection, performance appraisals, job description preparation, employee counseling, career coaching and termination meetings. Managing site staff, proactively identify and resolve issues, and work to ensure successful site operations.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOverseeing all payroll, absence tracking/approvals, new hire orientation, and training per operational needs.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCollaborating with investigators to ensure patient safety and meeting client goals and timelines.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEmploying strategic thinking and problem-solving skills to propose and implement risk mitigations.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eParticipating and presenting in management or site meetings.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform all other duties as required or assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Austin Wing","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A Bachelor’s degree AND 5+ years of clinical research experience or an equivalent combination of education and experience is required.\u0026nbsp; 2+ years of clinical research site management required. \u0026nbsp; Bi-lingual (English / Spanish) proficiency is required.\u003cbr\u003e\u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm).\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess strong organizational, time management, problem solving, and project management skills to meet project deadlines.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Site Director - Must be bilingual (English/Spanish)","url":"https://alcanzaclinical.pinpointhq.com/en/postings/2c3b1810-6758-4580-8c93-a298dcad4574","path":"/en/postings/2c3b1810-6758-4580-8c93-a298dcad4574","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"509633","requisition_id":"PIN-1572","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"30854","city":"Palmetto Bay","name":"Innovation - Palmetto Bay, FL","postal_code":"","province":"Florida"}},{"id":"503513","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. 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We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eClinical Research Coordinator (CRC)\u003c/strong\u003e works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. \u0026nbsp;\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties: \u003c/strong\u003eIn collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. 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ordering study specific supplies;]\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eScheduling subjects for study visits and conducts appointment reminders;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eBuilding/updating source as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eConducting monitoring visits and resolves issues as needed in a timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring study related reports and patient results are reviewed by investigator in a timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eFiling SAE/Deviation reports to Sponsor and IRB as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocumenting and reporting adverse events;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eReporting non-compliance to appropriate staff in timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining positive and effective communication with clients and team members;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAlways practicing ALCOAC principles with all documentation;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with study recruitment, patient enrollment, and tracking as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining confidentiality of patients, customers and company information, and;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming all other duties as requested or assigned.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePrepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay set up, train and maintain all technology needed for studies.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Nikki Shebelskie","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required.\u0026nbsp; Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus. \u003cbr\u003e \u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStrong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks, and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Coordinator","url":"https://alcanzaclinical.pinpointhq.com/en/postings/8cc05ac6-6e5c-4438-8c60-15002baf951d","path":"/en/postings/8cc05ac6-6e5c-4438-8c60-15002baf951d","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"512977","requisition_id":"PIN-1580","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"11667","city":"North Charleston","name":"Coastal Carolina Research Center | Charleston, SC","postal_code":"29405","province":"South Carolina"}},{"id":"506766","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. \u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003ePatient Liaison\u003c/strong\u003e is responsible for supporting onsite patient recruitment efforts by\u003cbr\u003econducting pre-qualification, pre-screening, and scheduling activities to ensure a smooth and efficient enrollment process.\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eExecute onsite patient pre-screening and a focus on pivoting qualified patients into active studies for dedicated and local sites should patient be willing to travel.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEvaluate eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with site clinic staff. Support patient path to enrollment, managing all follow up and communication including reminder calls, rescheduling, etc.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor/manage onsite patient screening visit schedule – schedule/ reschedule appointments as needed or requested.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOwn No-Show/DNQ tracking, triaging, optimization.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCapture/manage inbound physician referral leads.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAddress and resolve patient barriers to study entry by leveraging knowledge of site or sponsor-provided support services, such as transportation assistance and reimbursement programs.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsure timely and consistent updating to Clinical Conductor/CTMS – updating patient touches/patient profile statuses, etc.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCreate targeted call lists based on i/e criteria in CTMS to best target patient populations for call efficiency.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePosition shares accountability for regional recruitment results. Drive screening numbers to meet recruitment goals set by leadership. Assist with collection of performance metrics related to attribution capability for screening visits.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eImmediately notify RSLs and/or recruitment leadership of any barriers and/or challenges to screens scheduled or completed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAcquire and continuously update knowledge of clinical research studies, including detailed understanding of their inclusion and exclusion criteria.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eManage patient portal leads (central campaigns) to include review, calling and updating patient leads.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor status of Refer-A-Friend campaigns\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRepresent company with HCP referral partners for local support and relationship management.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSupport planning and participate in local community outreach events to engage/educate patients about clinical trials, as needed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with new recruiter training and retraining of current team members.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform all other duties that may be requested or assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Mary Love","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A high school diploma, or equivalent, AND a minimum of 5 years’ experience in a medical, healthcare, or medical research environment, or a similar field, or an equivalent combination of education and experience, is required.\u0026nbsp; MA, CNA, LPN/LVN, EMT or other medical license is preferred.\u0026nbsp; Experience with therapy areas, customer service, calendar management /scheduling and CTMS (Clinical Trial Management System) experience is highly preferred.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eRequired Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as email, electronic health records, and basic applications.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to type proficiently (40+ wpm).\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess strong organizational skills, attention to detail, and have basic math proficiency.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is highly preferred.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed listening skills and the ability to work well alone as well as in a team atmosphere. \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle multiple tasks and changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of honesty and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and help find solutions.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive patient health information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Patient Liaison - ( Patient Recruitment )","url":"https://alcanzaclinical.pinpointhq.com/en/postings/c2abe9d1-526c-45a0-a9d5-3bd7b5f82939","path":"/en/postings/c2abe9d1-526c-45a0-a9d5-3bd7b5f82939","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"513618","requisition_id":"PIN-1581","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"11667","city":"North Charleston","name":"Coastal Carolina Research Center | Charleston, SC","postal_code":"29405","province":"South Carolina"}},{"id":"507647","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eClinical Research Coordinator (CRC)\u003c/strong\u003e works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. \u0026nbsp;\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties: \u003c/strong\u003eIn collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eScreening of patients for study enrollment;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient consents;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient follow-up visits;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocumenting in source clinic charts;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEntering data in EDC and answers queries;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eObtaining vital signs and ECGs;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay perform basic lab procedures per protocol, such as:\u0026nbsp; blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRequesting and tracking medical record requests;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUpdating and maintaining logs, chart filings;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining \u0026amp; ordering study specific supplies;]\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eScheduling subjects for study visits and conducts appointment reminders;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eBuilding/updating source as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eConducting monitoring visits and resolves issues as needed in a timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring study related reports and patient results are reviewed by investigator in a timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eFiling SAE/Deviation reports to Sponsor and IRB as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocumenting and reporting adverse events;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eReporting non-compliance to appropriate staff in timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining positive and effective communication with clients and team members;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAlways practicing ALCOAC principles with all documentation;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with study recruitment, patient enrollment, and tracking as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining confidentiality of patients, customers and company information, and;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming all other duties as requested or assigned.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePrepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay set up, train and maintain all technology needed for studies.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Shannon Rodman","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required.\u0026nbsp; Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus. \u003cbr\u003e \u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStrong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks, and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Coordinator","url":"https://alcanzaclinical.pinpointhq.com/en/postings/a19819ff-6021-40e3-ad14-51f623a20e34","path":"/en/postings/a19819ff-6021-40e3-ad14-51f623a20e34","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"514462","requisition_id":"PIN-1567","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"85374","city":"Gilbert","name":"Phoenix Medical Trials - Gilbert, AZ","postal_code":"85295","province":"Arizona"}},{"id":"508580","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. \u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003ePatient Liaison\u003c/strong\u003e is responsible for supporting onsite patient recruitment efforts by\u003cbr\u003econducting pre-qualification, pre-screening, and scheduling activities to ensure a smooth and efficient enrollment process.\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eExecute onsite patient pre-screening and a focus on pivoting qualified patients into active studies for dedicated and local sites should patient be willing to travel.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEvaluate eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with site clinic staff. Support patient path to enrollment, managing all follow up and communication including reminder calls, rescheduling, etc.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor/manage onsite patient screening visit schedule – schedule/ reschedule appointments as needed or requested.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOwn No-Show/DNQ tracking, triaging, optimization.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCapture/manage inbound physician referral leads.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAddress and resolve patient barriers to study entry by leveraging knowledge of site or sponsor-provided support services, such as transportation assistance and reimbursement programs.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsure timely and consistent updating to Clinical Conductor/CTMS – updating patient touches/patient profile statuses, etc.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCreate targeted call lists based on i/e criteria in CTMS to best target patient populations for call efficiency.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePosition shares accountability for regional recruitment results. Drive screening numbers to meet recruitment goals set by leadership. Assist with collection of performance metrics related to attribution capability for screening visits.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eImmediately notify RSLs and/or recruitment leadership of any barriers and/or challenges to screens scheduled or completed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAcquire and continuously update knowledge of clinical research studies, including detailed understanding of their inclusion and exclusion criteria.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eManage patient portal leads (central campaigns) to include review, calling and updating patient leads.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor status of Refer-A-Friend campaigns\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRepresent company with HCP referral partners for local support and relationship management.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSupport planning and participate in local community outreach events to engage/educate patients about clinical trials, as needed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with new recruiter training and retraining of current team members.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform all other duties that may be requested or assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Carolyn Monden","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A high school diploma, or equivalent, AND a minimum of 5 years’ experience in a medical, healthcare, or medical research environment, or a similar field, or an equivalent combination of education and experience, is required.\u0026nbsp; MA, CNA, LPN/LVN, EMT or other medical license is preferred.\u0026nbsp; Experience with therapy areas, customer service, calendar management /scheduling and CTMS (Clinical Trial Management System) experience is highly preferred.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eRequired Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as email, electronic health records, and basic applications.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to type proficiently (40+ wpm).\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess strong organizational skills, attention to detail, and have basic math proficiency.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is highly preferred.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed listening skills and the ability to work well alone as well as in a team atmosphere. \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle multiple tasks and changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of honesty and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and help find solutions.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive patient health information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Patient Liaison (Patient Recruiter) ","url":"https://alcanzaclinical.pinpointhq.com/en/postings/0b372074-6dab-405f-9f4e-53c59c587f6f","path":"/en/postings/0b372074-6dab-405f-9f4e-53c59c587f6f","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"515338","requisition_id":"PIN-1576","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"19136","city":"Decatur","name":"Accel Research Sites - Decatur, GA","postal_code":"30030","province":"GA"}},{"id":"509647","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eInvestigational Product Coordinator \u003c/strong\u003eis responsible for preparing and dispensing study drug, providing drug-related information to subjects and staff in compliance with GCP, ICH, HIPAA, FDA, USP 797, USP 800, state Boards of Pharmacy, and company SOPs. \u0026nbsp;\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eUnder the direction of the Lead Research Pharmacist (or similar) and the Principal/Sub Investigators, conducts the following according to study protocol, company processes \u0026amp; procedures, and in compliance with GCP, ICH, HIPPA, FDA, USP 797, USP 800, state Boards of Pharmacy and company SOPs:\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Integration of investigational medication use, pharmacy workflow, subject medication safety activities and regulatory standards;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Coordinating, and advising site staff on drug distribution services for investigational medications;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Identify and justify needs for additional resources, or redeploying resources in new ways to meet needs;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Prepares, labels (if required) and dispenses investigational medications, and provides drug-related information and education for subjects and site staff;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Dispenses controlled substances as part of a research study.\u0026nbsp; Maintains appropriate inventory records, documentation of receipt and ensures proper storage conditions\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsures safety and care for all research subjects as it relates to investigational medication preparation and dispensing;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePromotes individual professional growth and development by meeting requirements for mandatory/continuing education and skills competency; supports department-based goals which contribute to the success of the organization; serves as mentor and resource to less experienced staff\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOther duties as assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Mary Rogers","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; An associate’s degree and 1+ years’ related experience, OR an equivalent combination of education and experience, is required. \u0026nbsp; Certified Pharmacy Technician (CPhT) credential is required.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u0026nbsp; \u003cbr\u003e\u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, web applications,\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStrong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, management, and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Certified Pharmacy Technician ","url":"https://alcanzaclinical.pinpointhq.com/en/postings/edd434a2-2ede-46a2-bb3c-d9e57c7810b1","path":"/en/postings/edd434a2-2ede-46a2-bb3c-d9e57c7810b1","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"516227","requisition_id":"PIN-1597","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"30852","city":"Katy","name":"Olympus - Katy, TX","postal_code":"","province":"Texas"}},{"id":"511522","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eClinical Research Nurse \u003c/strong\u003eworks to ensure the execution of assigned studies, and performs clinical procedures, such as venipunctures, injections, prep or mixing of investigational study drugs and infusions, under the scope of the study protocol and in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.\u003c/div\u003e","employment_type":"part_time","employment_type_text":"Part Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties: \u003c/strong\u003eIn collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eUnder the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes \u0026amp; procedures, and in compliance with FDA, GCP, ICH regulations and guidelines:\u0026nbsp;\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eScreening of patients for study enrollment;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient consents;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient follow-up visits;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocumenting in source clinic charts;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEntering data in EDC and answers queries;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eObtaining vital signs and ECGs;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay perform basic lab procedures per protocol, such as:\u0026nbsp; blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming procedures commensurate with licensure including vitals, ECGs/EKGs, venipunctures, injections, infusions, mixing drug and/or dispense investigational product; etc.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRequesting and tracking medical record requests;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUpdating and maintaining logs, chart filings;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining \u0026amp; ordering study specific supplies;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eScheduling subjects for study visits and conducts appointment reminders;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eBuilding/updating source as needed;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eConducting monitoring visits and resolves issues as needed in a timely manner;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring study related reports and patient results are reviewed by investigator in a timely manner;\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Filing SAE/Deviation reports to Sponsor and IRB as needed;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Documenting and reporting adverse events;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Reporting non-compliance to appropriate staff in timely manner;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Maintaining positive and effective communication with clients and team members;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Always practicing ALCOAC principles with all documentation;\u003cbr\u003e\u0026nbsp;\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eBe thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePrepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay set up, train and maintain all technology needed for studies.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with study recruitment, patient enrollment, and tracking as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining confidentiality of patients, customers and company information, and;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming all other duties as requested or assigned.\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Rebecca Carrillo","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A Bachelor’s degree in Nursing (BSN) AND a minimum of 1 year of clinical experience, OR an equivalent combination of education and experience, is required.\u0026nbsp; An active, unrestricted RN license, in state of work location, is required.\u0026nbsp; BLS certification required.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u0026nbsp; \u003cbr\u003e \u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003cbr\u003e\u003c/strong\u003e\u003cbr\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with performing clinical procedures such as injections, vitals, EKGs, phlebotomy, infusions, etc. is required. \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStrong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks, and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Registered Nurse ( PT WeekDay)","url":"https://alcanzaclinical.pinpointhq.com/en/postings/3572ab02-0180-4d46-89c1-55c9d64fe717","path":"/en/postings/3572ab02-0180-4d46-89c1-55c9d64fe717","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"518043","requisition_id":"PIN-1605","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"12394","city":"Roslindale","name":"Boston Clinical Trials | Roslindale, MA","postal_code":"02131","province":"Massachusetts"}},{"id":"511534","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eClinical Research Nurse \u003c/strong\u003eworks to ensure the execution of assigned studies, and performs clinical procedures, such as venipunctures, injections, prep or mixing of investigational study drugs and infusions, under the scope of the study protocol and in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.\u003c/div\u003e","employment_type":"part_time","employment_type_text":"Part Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties: \u003c/strong\u003eIn collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eUnder the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes \u0026amp; procedures, and in compliance with FDA, GCP, ICH regulations and guidelines:\u0026nbsp;\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eScreening of patients for study enrollment;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient consents;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient follow-up visits;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocumenting in source clinic charts;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEntering data in EDC and answers queries;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eObtaining vital signs and ECGs;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay perform basic lab procedures per protocol, such as:\u0026nbsp; blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming procedures commensurate with licensure including vitals, ECGs/EKGs, venipunctures, injections, infusions, mixing drug and/or dispense investigational product; etc.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRequesting and tracking medical record requests;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUpdating and maintaining logs, chart filings;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining \u0026amp; ordering study specific supplies;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eScheduling subjects for study visits and conducts appointment reminders;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eBuilding/updating source as needed;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eConducting monitoring visits and resolves issues as needed in a timely manner;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring study related reports and patient results are reviewed by investigator in a timely manner;\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Filing SAE/Deviation reports to Sponsor and IRB as needed;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Documenting and reporting adverse events;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Reporting non-compliance to appropriate staff in timely manner;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Maintaining positive and effective communication with clients and team members;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Always practicing ALCOAC principles with all documentation;\u003cbr\u003e\u0026nbsp;\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eBe thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePrepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay set up, train and maintain all technology needed for studies.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with study recruitment, patient enrollment, and tracking as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining confidentiality of patients, customers and company information, and;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming all other duties as requested or assigned.\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A Bachelor’s degree in Nursing (BSN) AND a minimum of 1 year of clinical experience, OR an equivalent combination of education and experience, is required.\u0026nbsp; An active, unrestricted RN license, in state of work location, is required.\u0026nbsp; BLS certification required.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u0026nbsp; \u003cbr\u003e \u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003cbr\u003e\u003c/strong\u003e\u003cbr\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with performing clinical procedures such as injections, vitals, EKGs, phlebotomy, infusions, etc. is required. \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStrong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks, and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Registered Nurse ( PT WeekDay)","url":"https://alcanzaclinical.pinpointhq.com/en/postings/6381754f-0258-42f2-94d2-ac9c941e62df","path":"/en/postings/6381754f-0258-42f2-94d2-ac9c941e62df","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"518054","requisition_id":"PIN-1606","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"11665","city":" Methuen","name":"ActivMed Practices \u0026 Research | Methuen, MA","postal_code":"01844","province":"Massachusetts"}},{"id":"511593","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. \u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eIntake Specialist \u003c/strong\u003eis the first point of contact at the site making this a crucial role. Excellence in customer service is a must as this role is responsible for providing a pleasant experience for the volunteers by providing a warm friendly greeting, answering any questions, addressing their concerns and providing assistance. It is important that this role be the relationship bridge between recruitment and the clinic staff to ensure their experience is enjoyable from the first phone call to the last visit of the trial.\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eThis position is the front line of support for the site and may perform a variety of tasks, including but not limited to:\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eGreeting volunteers and other visitors as soon as they arrive;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eObtain/verify proper identification of each volunteer and upload into CTMS;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePrepare, provide and explain the necessary documents for them to complete and read.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eProvide answers, information, and conversation to the volunteers making them feel comfortable and confident in their decision to participate in a trial;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAnswer inbound calls and emails with a high level of customer service;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePlace reminder calls to confirm scheduled appointment (according to guidelines);\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssist with appointment rescheduling as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCall volunteers who are 15 minutes or more late to arrive for their appointment;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eNotify appropriate staff of volunteer’s arrival and ensure they promptly come to greet them;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete visits in the CTMS with strong attention to detail to ensure the maximum revenue is captured for billing.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUpdates CTMS with subject profile(demographics) and file/upload W9 form;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssign payment cards and issue stipend payments following visit completion;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCoordinates / schedules transportation for volunteers;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintain tracker of no-show volunteers until reschedule has been completed;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintain tracker of screening volunteers without an upcoming scheduled appointment;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSend weekly reports of appointment statuses to clinic staff to avoid missed appointments;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintain a list of studies conducted at site and have general understanding of each;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSubmit medical records requests and track their progress;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSorting and distributing incoming mail; coordinating postage details \u0026amp; pick ups as needed for all outbound mail;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePlacing supply orders;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCompiling office correspondence, filing, copying, collating, scanning as needed;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssist with preparing materials for study startup / SIVs;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with special projects as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforms all other duties that may be requested or assigned.\u003c/li\u003e\u003c/ul\u003e\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Heather Fasczewski","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; An Associate’s degree and a minimum of 3 years’ experience in customer service, administration or sales, or an equivalent combination of education and experience, is required. Must have well-developed customer service skills. Experience with calendar management \u0026amp; scheduling is preferred. 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We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eVice President of Operational Finance\u003c/strong\u003e provides enterprise-wide leadership of operational finance across a multi-site clinical research network. This role owns the site profitability insights, cost and margin management, and operational KPI governance; partners closely with Operations leadership to translate study performance and patient journey metrics into financial outcomes; and leads the annual planning process, rolling forecasts, scenario and sensitivity analysis, and executive reporting. 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Escalate issues as appropriate or needed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsure compliance with regulatory guidelines and company policies.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eParticipate and present in team, department, management or site meetings.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintain a positive, results-oriented work environment, build partnerships within the team and across the organization at large, and model teamwork.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform all other duties that may be requested or assigned\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Jeff Irving","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A bachelor’s degree in finance or accounting AND 10+ years of progressive finance leadership experience including multi-site operational finance, and specifically within either clinical research or healthcare services, and within privity equity backed environments, is required. 2+ years of people management experience is required. 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We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eClinical Research Coordinator (CRC)\u003c/strong\u003e works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. \u0026nbsp;\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties: \u003c/strong\u003eIn collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eScreening of patients for study enrollment;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient consents;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient follow-up visits;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocumenting in source clinic charts;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEntering data in EDC and answers queries;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eObtaining vital signs and ECGs;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay perform basic lab procedures per protocol, such as:\u0026nbsp; blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRequesting and tracking medical record requests;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUpdating and maintaining logs, chart filings;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining \u0026amp; ordering study specific supplies;]\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eScheduling subjects for study visits and conducts appointment reminders;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eBuilding/updating source as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eConducting monitoring visits and resolves issues as needed in a timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring study related reports and patient results are reviewed by investigator in a timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eFiling SAE/Deviation reports to Sponsor and IRB as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocumenting and reporting adverse events;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eReporting non-compliance to appropriate staff in timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining positive and effective communication with clients and team members;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAlways practicing ALCOAC principles with all documentation;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with study recruitment, patient enrollment, and tracking as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining confidentiality of patients, customers and company information, and;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming all other duties as requested or assigned.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePrepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay set up, train and maintain all technology needed for studies.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required.\u0026nbsp; Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus. \u003cbr\u003e \u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStrong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks, and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Coordinator ","url":"https://alcanzaclinical.pinpointhq.com/en/postings/fc9bd41e-237d-4ad4-b11a-6a3a52d526f1","path":"/en/postings/fc9bd41e-237d-4ad4-b11a-6a3a52d526f1","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"520053","requisition_id":"PIN-1613","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"32154","city":"Kansas City","name":"Kansas City Research Institute - Kansas City, MO","postal_code":"64131","province":"Missouri"}},{"id":"513567","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eClinical Research Coordinator (CRC)\u003c/strong\u003e works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. \u0026nbsp;\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties: \u003c/strong\u003eIn collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eScreening of patients for study enrollment;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient consents;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient follow-up visits;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocumenting in source clinic charts;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEntering data in EDC and answers queries;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eObtaining vital signs and ECGs;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay perform basic lab procedures per protocol, such as:\u0026nbsp; blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRequesting and tracking medical record requests;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUpdating and maintaining logs, chart filings;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining \u0026amp; ordering study specific supplies;]\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eScheduling subjects for study visits and conducts appointment reminders;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eBuilding/updating source as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eConducting monitoring visits and resolves issues as needed in a timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring study related reports and patient results are reviewed by investigator in a timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eFiling SAE/Deviation reports to Sponsor and IRB as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocumenting and reporting adverse events;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eReporting non-compliance to appropriate staff in timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining positive and effective communication with clients and team members;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAlways practicing ALCOAC principles with all documentation;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with study recruitment, patient enrollment, and tracking as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining confidentiality of patients, customers and company information, and;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming all other duties as requested or assigned.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePrepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay set up, train and maintain all technology needed for studies.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Brie jackson ","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required.\u0026nbsp; Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus. \u003cbr\u003e \u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStrong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks, and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Coordinator ","url":"https://alcanzaclinical.pinpointhq.com/en/postings/ac578255-b1ed-4e7b-aecf-e7a0b251c96b","path":"/en/postings/ac578255-b1ed-4e7b-aecf-e7a0b251c96b","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"520063","requisition_id":"PIN-1614","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"77963","city":"Clearwater","name":"Tampa Bay Medical Research - Clearwater","postal_code":"33761","province":"Florida"}},{"id":"517175","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eClinical Research Nurse \u003c/strong\u003eworks to ensure the execution of assigned studies, and performs clinical procedures, such as venipunctures, injections, prep or mixing of investigational study drugs and infusions, under the scope of the study protocol and in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties: \u003c/strong\u003eIn collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eUnder the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes \u0026amp; procedures, and in compliance with FDA, GCP, ICH regulations and guidelines:\u0026nbsp;\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eScreening of patients for study enrollment;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient consents;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient follow-up visits;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocumenting in source clinic charts;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEntering data in EDC and answers queries;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eObtaining vital signs and ECGs;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStarting IVs\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay perform basic lab procedures per protocol, such as:\u0026nbsp; blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming procedures commensurate with licensure including vitals, ECGs/EKGs, venipunctures, injections, infusions, mixing drug and/or dispense investigational product; etc.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRequesting and tracking medical record requests;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUpdating and maintaining logs, chart filings;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining \u0026amp; ordering study specific supplies;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eScheduling subjects for study visits and conducts appointment reminders;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eBuilding/updating source as needed;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eConducting monitoring visits and resolves issues as needed in a timely manner;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring study related reports and patient results are reviewed by investigator in a timely manner;\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Filing SAE/Deviation reports to Sponsor and IRB as needed;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Documenting and reporting adverse events;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Reporting non-compliance to appropriate staff in timely manner;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Maintaining positive and effective communication with clients and team members;\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eo\u0026nbsp; \u0026nbsp; Always practicing ALCOAC principles with all documentation;\u003cbr\u003e\u0026nbsp;\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eBe thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePrepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay set up, train and maintain all technology needed for studies.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with study recruitment, patient enrollment, and tracking as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining confidentiality of patients, customers and company information, and;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming all other duties as requested or assigned.\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Adrianna Doggett","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A Bachelor’s degree in Nursing (BSN) AND a minimum of 1 year of clinical experience, OR an equivalent combination of education and experience, is required.\u0026nbsp; An active, unrestricted RN license, in state of work location, is required.\u0026nbsp; BLS certification required.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u0026nbsp; \u003cbr\u003e \u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with performing clinical procedures such as injections, vitals, EKGs, phlebotomy, infusions, etc. is required. \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStrong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks, and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Registered Nurse","url":"https://alcanzaclinical.pinpointhq.com/en/postings/d8462104-6a60-4205-921b-f329a2576a30","path":"/en/postings/d8462104-6a60-4205-921b-f329a2576a30","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"492014","requisition_id":"PIN-1505","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"11668","city":"Charlottesville ","name":"Charlottesville Medical Research Center | Charlottesville, VA","postal_code":"22911","province":"Virginia"}},{"id":"517254","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. \u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eResearch Assistant (RA) \u003c/strong\u003eprovides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.\u0026nbsp; The RA performs clinical, lab, and administrative tasks as needed for the successful operation of the clinical research site.\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties: \u003c/strong\u003eIn collaboration with other members of the clinical research site team, assists with the execution of assigned studies, and support functions as needed. Responsibilities may include but are not limited to:\u0026nbsp;\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eUnder the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol:\u0026nbsp;\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eAssists with the basic screening of patients for study enrollment;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssists with patient follow-up visits;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocuments in source clinic charts;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnters data in EDC and answers queries;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eObtains vital signs and ECGs;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay perform blood draws;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform basic lab procedures per protocol, such as:\u0026nbsp; blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRequest and track medical record requests;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnters data in EDC and answers queries;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSchedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed;\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.\u0026nbsp; \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssists the CRC and/or Manager with study recruitment, patient enrollment, and tracking as needed;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintains strict confidentiality of patients, employees, customers and company information at all times and adheres to HIPAA Guidelines; and\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform all other duties as requested or assigned.\u0026nbsp;\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"colleen Figueroa","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e: A High School diploma and 1 year of administrative / clinical experience is required. \u0026nbsp; 1 year or more years of clinical research or clinical experience is preferred.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eRequired Skills:\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm).\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess strong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Assistant/ Medical Assistant ","url":"https://alcanzaclinical.pinpointhq.com/en/postings/62c13403-154b-40e0-bee3-360f0ce7c8f8","path":"/en/postings/62c13403-154b-40e0-bee3-360f0ce7c8f8","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"523387","requisition_id":"PIN-1616","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"19128","city":"Lakeland","name":"Accel Research Sites - Lakeland, FL","postal_code":"33803","province":"FL"}},{"id":"517771","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eClinical Research Coordinator (CRC)\u003c/strong\u003e works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. \u0026nbsp;\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties: \u003c/strong\u003eIn collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eScreening of patients for study enrollment;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient consents;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePatient follow-up visits;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocumenting in source clinic charts;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEntering data in EDC and answers queries;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eObtaining vital signs and ECGs;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay perform basic lab procedures per protocol, such as:\u0026nbsp; blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRequesting and tracking medical record requests;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUpdating and maintaining logs, chart filings;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining \u0026amp; ordering study specific supplies;]\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eScheduling subjects for study visits and conducts appointment reminders;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eBuilding/updating source as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eConducting monitoring visits and resolves issues as needed in a timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring study related reports and patient results are reviewed by investigator in a timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eFiling SAE/Deviation reports to Sponsor and IRB as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eDocumenting and reporting adverse events;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eReporting non-compliance to appropriate staff in timely manner;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining positive and effective communication with clients and team members;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAlways practicing ALCOAC principles with all documentation;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with study recruitment, patient enrollment, and tracking as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining confidentiality of patients, customers and company information, and;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming all other duties as requested or assigned.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePrepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay set up, train and maintain all technology needed for studies.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Adrianna Doggett","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required.\u0026nbsp; Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus. \u003cbr\u003e \u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStrong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks, and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Coordinator","url":"https://alcanzaclinical.pinpointhq.com/en/postings/8f5b59b0-f028-4d3a-8054-473abf27d250","path":"/en/postings/8f5b59b0-f028-4d3a-8054-473abf27d250","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"523866","requisition_id":"PIN-1604","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"11668","city":"Charlottesville ","name":"Charlottesville Medical Research Center | Charlottesville, VA","postal_code":"22911","province":"Virginia"}},{"id":"518397","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. \u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003ePatient Liaison\u003c/strong\u003e is responsible for supporting onsite patient recruitment efforts by conducting pre-qualification, pre-screening, and scheduling activities to ensure a smooth and efficient enrollment process.\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eExecute onsite patient pre-screening and a focus on pivoting qualified patients into active studies for dedicated and local sites should patient be willing to travel.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEvaluate eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with site clinic staff. Support patient path to enrollment, managing all follow up and communication including reminder calls, rescheduling, etc.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor/manage onsite patient screening visit schedule – schedule/ reschedule appointments as needed or requested.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOwn No-Show/DNQ tracking, triaging, optimization.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCapture/manage inbound physician referral leads.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAddress and resolve patient barriers to study entry by leveraging knowledge of site or sponsor-provided support services, such as transportation assistance and reimbursement programs.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsure timely and consistent updating to Clinical Conductor/CTMS – updating patient touches/patient profile statuses, etc.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCreate targeted call lists based on i/e criteria in CTMS to best target patient populations for call efficiency.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePosition shares accountability for regional recruitment results. Drive screening numbers to meet recruitment goals set by leadership. Assist with collection of performance metrics related to attribution capability for screening visits.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eImmediately notify RSLs and/or recruitment leadership of any barriers and/or challenges to screens scheduled or completed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAcquire and continuously update knowledge of clinical research studies, including detailed understanding of their inclusion and exclusion criteria.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eManage patient portal leads (central campaigns) to include review, calling and updating patient leads.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor status of Refer-A-Friend campaigns\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRepresent company with HCP referral partners for local support and relationship management.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSupport planning and participate in local community outreach events to engage/educate patients about clinical trials, as needed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with new recruiter training and retraining of current team members.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform all other duties that may be requested or assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Kathleen Valcich","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A high school diploma, or equivalent, AND a minimum of 5 years’ experience in a medical, healthcare, or medical research environment, or a similar field, or an equivalent combination of education and experience, is required.\u0026nbsp; MA, CNA, LPN/LVN, EMT or other medical license is preferred.\u0026nbsp; Experience with therapy areas, customer service, calendar management /scheduling and CTMS (Clinical Trial Management System) experience is highly preferred.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eRequired Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as email, electronic health records, and basic applications.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to type proficiently (40+ wpm).\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess strong organizational skills, attention to detail, and have basic math proficiency.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is highly preferred.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed listening skills and the ability to work well alone as well as in a team atmosphere. \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle multiple tasks and changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of honesty and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and help find solutions.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive patient health information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Patient Liaison (Patient Recruiter)","url":"https://alcanzaclinical.pinpointhq.com/en/postings/d4c9d59a-2184-4efd-91cc-2fb761e6db0a","path":"/en/postings/d4c9d59a-2184-4efd-91cc-2fb761e6db0a","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"524443","requisition_id":"PIN-1619","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"11665","city":" Methuen","name":"ActivMed Practices \u0026 Research | Methuen, MA","postal_code":"01844","province":"Massachusetts"}},{"id":"518590","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. \u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eIntake Specialist \u003c/strong\u003eis the first point of contact at the site making this a crucial role. Excellence in customer service is a must as this role is responsible for providing a pleasant experience for the volunteers by providing a warm friendly greeting, answering any questions, addressing their concerns and providing assistance. It is important that this role be the relationship bridge between recruitment and the clinic staff to ensure their experience is enjoyable from the first phone call to the last visit of the trial.\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eThis position is the front line of support for the site and may perform a variety of tasks, including but not limited to:\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eGreeting volunteers and other visitors as soon as they arrive;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eObtain/verify proper identification of each volunteer and upload into CTMS;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePrepare, provide and explain the necessary documents for them to complete and read.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eProvide answers, information, and conversation to the volunteers making them feel comfortable and confident in their decision to participate in a trial;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAnswer inbound calls and emails with a high level of customer service;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePlace reminder calls to confirm scheduled appointment (according to guidelines);\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssist with appointment rescheduling as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCall volunteers who are 15 minutes or more late to arrive for their appointment;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eNotify appropriate staff of volunteer’s arrival and ensure they promptly come to greet them;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete visits in the CTMS with strong attention to detail to ensure the maximum revenue is captured for billing.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUpdates CTMS with subject profile(demographics) and file/upload W9 form;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssign payment cards and issue stipend payments following visit completion;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCoordinates / schedules transportation for volunteers;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintain tracker of no-show volunteers until reschedule has been completed;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintain tracker of screening volunteers without an upcoming scheduled appointment;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSend weekly reports of appointment statuses to clinic staff to avoid missed appointments;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintain a list of studies conducted at site and have general understanding of each;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSubmit medical records requests and track their progress;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSorting and distributing incoming mail; coordinating postage details \u0026amp; pick ups as needed for all outbound mail;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePlacing supply orders;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCompiling office correspondence, filing, copying, collating, scanning as needed;\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssist with preparing materials for study startup / SIVs;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with special projects as needed;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforms all other duties that may be requested or assigned.\u003c/li\u003e\u003c/ul\u003e\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Rebecca Laguna Carrillo","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; An Associate’s degree and a minimum of 3 years’ experience in customer service, administration or sales, or an equivalent combination of education and experience, is required. Must have well-developed customer service skills. Experience with calendar management \u0026amp; scheduling is preferred. 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We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. \u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003ePatient Liaison\u003c/strong\u003e is responsible for supporting onsite patient recruitment efforts by\u003cbr\u003econducting pre-qualification, pre-screening, and scheduling activities to ensure a smooth and efficient enrollment process.\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eExecute onsite patient pre-screening and a focus on pivoting qualified patients into active studies for dedicated and local sites should patient be willing to travel.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEvaluate eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with site clinic staff. Support patient path to enrollment, managing all follow up and communication including reminder calls, rescheduling, etc.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor/manage onsite patient screening visit schedule – schedule/ reschedule appointments as needed or requested.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOwn No-Show/DNQ tracking, triaging, optimization.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCapture/manage inbound physician referral leads.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAddress and resolve patient barriers to study entry by leveraging knowledge of site or sponsor-provided support services, such as transportation assistance and reimbursement programs.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsure timely and consistent updating to Clinical Conductor/CTMS – updating patient touches/patient profile statuses, etc.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCreate targeted call lists based on i/e criteria in CTMS to best target patient populations for call efficiency.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePosition shares accountability for regional recruitment results. Drive screening numbers to meet recruitment goals set by leadership. Assist with collection of performance metrics related to attribution capability for screening visits.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eImmediately notify RSLs and/or recruitment leadership of any barriers and/or challenges to screens scheduled or completed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAcquire and continuously update knowledge of clinical research studies, including detailed understanding of their inclusion and exclusion criteria.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eManage patient portal leads (central campaigns) to include review, calling and updating patient leads.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor status of Refer-A-Friend campaigns\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eRepresent company with HCP referral partners for local support and relationship management.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eSupport planning and participate in local community outreach events to engage/educate patients about clinical trials, as needed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay assist with new recruiter training and retraining of current team members.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform all other duties that may be requested or assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Carolyn Monden","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A high school diploma, or equivalent, AND a minimum of 5 years’ experience in a medical, healthcare, or medical research environment, or a similar field, or an equivalent combination of education and experience, is required.\u0026nbsp; MA, CNA, LPN/LVN, EMT or other medical license is preferred.\u0026nbsp; Experience with therapy areas, customer service, calendar management /scheduling and CTMS (Clinical Trial Management System) experience is highly preferred.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eRequired Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as email, electronic health records, and basic applications.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to type proficiently (40+ wpm).\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess strong organizational skills, attention to detail, and have basic math proficiency.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp; Bi-lingual (English / Spanish) proficiency is highly preferred.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed listening skills and the ability to work well alone as well as in a team atmosphere. \u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle multiple tasks and changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of honesty and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and help find solutions.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive patient health information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Patient Liaison (Patient Recruiter) ","url":"https://alcanzaclinical.pinpointhq.com/en/postings/a240f0c5-2a07-45ae-b9ff-e1f96a76b765","path":"/en/postings/a240f0c5-2a07-45ae-b9ff-e1f96a76b765","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"526039","requisition_id":"PIN-1615","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"33023","city":"Woodstock","name":"North Georgia Clinical Research - Woodstock, GA","postal_code":"30189","province":"Georgia"}},{"id":"520102","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. 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Join us as we continue to grow.\u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eInvestigational Product Coordinator \u003c/strong\u003eis responsible for preparing and dispensing study drug, providing drug-related information to subjects and staff in compliance with GCP, ICH, HIPAA, FDA, USP 797, USP 800, state Boards of Pharmacy, and company SOPs. \u0026nbsp;\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cdiv\u003e\u003c!--block--\u003eUnder the direction of the Lead Research Pharmacist (or similar) and the Principal/Sub Investigators, conducts the following according to study protocol, company processes \u0026amp; procedures, and in compliance with GCP, ICH, HIPPA, FDA, USP 797, USP 800, state Boards of Pharmacy and company SOPs:\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Integration of investigational medication use, pharmacy workflow, subject medication safety activities and regulatory standards;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Coordinating, and advising site staff on drug distribution services for investigational medications;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Identify and justify needs for additional resources, or redeploying resources in new ways to meet needs;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Prepares, labels (if required) and dispenses investigational medications, and provides drug-related information and education for subjects and site staff;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003e\u0026nbsp;Dispenses controlled substances as part of a research study.\u0026nbsp; Maintains appropriate inventory records, documentation of receipt and ensures proper storage conditions\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsures safety and care for all research subjects as it relates to investigational medication preparation and dispensing;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePromotes individual professional growth and development by meeting requirements for mandatory/continuing education and skills competency; supports department-based goals which contribute to the success of the organization; serves as mentor and resource to less experienced staff\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOther duties as assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Harri Ann Turnipseed","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; An associate’s degree and 1+ years’ related experience, OR an equivalent combination of education and experience, is required. \u0026nbsp; 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Managing site staff, proactively identify and resolve issues, and work to ensure successful site operations.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eOverseeing all payroll, absence tracking/approvals, new hire orientation, and training per operational needs.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eCollaborating with investigators to ensure patient safety and meeting client goals and timelines.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEmploying strategic thinking and problem-solving skills to propose and implement risk mitigations.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eParticipating and presenting in management or site meetings.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerform all other duties as required or assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Kara Bardram","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; A Bachelor’s degree AND 5+ years of clinical research experience or an equivalent combination of education and experience is required.\u0026nbsp; 2+ years of management experience required.\u0026nbsp; Clinical research site management experience required. \u0026nbsp; Bi-lingual (English / Spanish) proficiency is a plus.\u003cbr\u003e\u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Required Skills:\u0026nbsp;\u003c/strong\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm).\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess strong organizational, time management, problem solving, and project management skills to meet project deadlines.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to work under minimal supervision, identify problems and implement solutions.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Clinical Research Site Director","url":"https://alcanzaclinical.pinpointhq.com/en/postings/28b07a39-e87a-4fa4-b271-043e9a2aaef1","path":"/en/postings/28b07a39-e87a-4fa4-b271-043e9a2aaef1","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"482599","requisition_id":"PIN-1471","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"11668","city":"Charlottesville ","name":"Charlottesville Medical Research Center | Charlottesville, VA","postal_code":"22911","province":"Virginia"}},{"id":"523267","benefits":"\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eFull-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.\u003c/li\u003e\u003c/ul\u003e\u003cdiv\u003e\u003c!--block--\u003e\u003cbr\u003e\u003c/div\u003e","benefits_header":"Benefits","compensation":null,"compensation_minimum":null,"compensation_maximum":null,"compensation_currency":null,"compensation_frequency":null,"compensation_visible":false,"deadline_at":null,"description":"\u003cdiv\u003e\u003c!--block--\u003eAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. \u003cbr\u003e\u003cbr\u003eThe \u003cstrong\u003eLab Coordinator\u003c/strong\u003e works to ensure the execution of assigned lab procedures in compliance with GCP, ICH, FED and HIPAA regulations, company SOPs, and policies. \u0026nbsp;\u003c/div\u003e","employment_type":"full_time","employment_type_text":"Full Time","key_responsibilities":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eEssential Job Duties: \u003c/strong\u003eResponsibilities may include but are not limited to:\u003cbr\u003e\u003cbr\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eDraw and process specimens according to each trial’s requirements\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAssist with specimen shipments to central labs and ensure proper shipping methods have been observed\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor expiration dates on lab equipment and supplies\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eUnpack and put away incoming lab supply shipments\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMonitor and maintain both general and study-specific lab inventory, and ensure study-specific lab supplies are ready for new study start-up\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eTransport samples\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eProvide mentoring to new hires and allow them to shadow you as they learn.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eComplete and renew CITI GCP and IATA training as required.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAttend SIVs when needed, and complete all sponsor-required lab training.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMay support other clinical research-related activities such as recruitment, EDC and QA/Chart review as needed.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eEnsuring compliance with company SOPs, FDA/HIPAA regulations, ICF documentation, and GCP guidelines\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMaintaining confidentiality of patients, customers, and company information, and\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003ePerforming other related activities as assigned.\u003c/li\u003e\u003c/ul\u003e","key_responsibilities_header":"Key Responsibilities","reporting_to":"Andrew Rodriguez","skills_knowledge_expertise":"\u003cdiv\u003e\u003c!--block--\u003e\u003cstrong\u003eMinimum Qualifications\u003c/strong\u003e:\u0026nbsp; High School diploma or equivalent and a minimum of 1 year of clinical laboratory processing experience is required. Associates degree is preferred.\u0026nbsp; Bilingual (English/Spanish) skills are a plus. \u003cbr\u003e \u003cbr\u003e \u003cstrong\u003eRequired Skills:\u0026nbsp;\u003cbr\u003e\u003c/strong\u003e\u003cbr\u003e\u003c/div\u003e\u003cul\u003e\u003cli\u003e\u003c!--block--\u003eProficiency with computer applications such as Microsoft applications, email, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eStrong organizational skills and attention to detail.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed written and verbal communication skills.\u0026nbsp;\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eWell-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to effectively handle multiple tasks and adapt to changes in workloads and priorities.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust be professional, respectful of others, self-motivated, and have a strong work ethic.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eMust possess a high degree of integrity and dependability.\u003c/li\u003e\u003cli\u003e\u003c!--block--\u003eAbility to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.\u003c/li\u003e\u003c/ul\u003e","skills_knowledge_expertise_header":"Skills, Knowledge and Expertise","title":"Lab Coordinator / Phlebotomist - Bilingual required (English/Spanish)","url":"https://alcanzaclinical.pinpointhq.com/en/postings/426027f2-1239-467e-a251-7c56b507bdcc","path":"/en/postings/426027f2-1239-467e-a251-7c56b507bdcc","workplace_type":"onsite","workplace_type_text":"Onsite","job":{"id":"498626","requisition_id":"PIN-1539","department":{"id":"21118","name":"Operations "},"division":null,"structure_custom_group_one":null},"location":{"id":"32153","city":"Mayaguez","name":"FDI Clinical Research - Mayaguez","postal_code":"","province":"Puerto Rico"}}]}