University of Arizona
Overview
Clinical Research Coordinator I – University of Arizona. This position coordinates a clinical trial patient through protocol-required procedures, including obtaining consent, screening, data collection and entry, and follow-up for all patients enrolled in assigned clinical trials. The coordinator acts as a liaison among regulatory, research, clinic, clinical faculty, and sponsor staff to carry out events outlined in protocol calendars, including data entry. The role supports the clinical research protocols from project initiation through study closure and, in the assigned disease areas (sleep, circadian, and mental health), develops knowledge of clinical research coordinator responsibilities. Responsibilities
Administer clinical tests and questionnaires as part of research protocols (assessments of sleep, circadian rhythms, mental health, cognitive functioning). Enter data for clinical study protocols and prepare reports. Prepare documents for submission to Research Intake and IRB, including protocols and consent forms, working with faculty, residents, external sponsors, and internal departments. Assist in research coordination with administrative support, schedule coordination, intake, and maintaining records/files. Occasionally work evenings and/or weekends as some activities occur outside standard hours. Conduct and review recruitment activities, including community-based recruitment and coordination with Psychiatry clinics. Work closely with participants to guide them through protocol elements of the study. Assist with administrative tasks within the research program, including purchasing and receipts. Knowledge, Skills & Abilities
Strong interpersonal, communication, and problem-saving skills. Excellent organizational skills. Attention to detail. Ability to multitask using time management skills. Comfortable navigating electronic databases. Other tasks as assigned. Minimum Qualifications
Bachelor’s degree or equivalent combination of education and experience. Up to 1 year of relevant work experience may be required. Preferred Qualifications
Experience working or volunteering directly with patients in a healthcare setting, or with human subjects. Experience with mental health conditions and/or sleep or circadian research. Comfort administering sensitive mental health assessments. CCRC training. Experience with federal regulation adherence. Additional Information
The posting includes standard compensation and benefits information; refer to the official UA job posting for details. The University of Arizona is an equal opportunity employer and a member of the AA/EOE workforce.
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Clinical Research Coordinator I – University of Arizona. This position coordinates a clinical trial patient through protocol-required procedures, including obtaining consent, screening, data collection and entry, and follow-up for all patients enrolled in assigned clinical trials. The coordinator acts as a liaison among regulatory, research, clinic, clinical faculty, and sponsor staff to carry out events outlined in protocol calendars, including data entry. The role supports the clinical research protocols from project initiation through study closure and, in the assigned disease areas (sleep, circadian, and mental health), develops knowledge of clinical research coordinator responsibilities. Responsibilities
Administer clinical tests and questionnaires as part of research protocols (assessments of sleep, circadian rhythms, mental health, cognitive functioning). Enter data for clinical study protocols and prepare reports. Prepare documents for submission to Research Intake and IRB, including protocols and consent forms, working with faculty, residents, external sponsors, and internal departments. Assist in research coordination with administrative support, schedule coordination, intake, and maintaining records/files. Occasionally work evenings and/or weekends as some activities occur outside standard hours. Conduct and review recruitment activities, including community-based recruitment and coordination with Psychiatry clinics. Work closely with participants to guide them through protocol elements of the study. Assist with administrative tasks within the research program, including purchasing and receipts. Knowledge, Skills & Abilities
Strong interpersonal, communication, and problem-saving skills. Excellent organizational skills. Attention to detail. Ability to multitask using time management skills. Comfortable navigating electronic databases. Other tasks as assigned. Minimum Qualifications
Bachelor’s degree or equivalent combination of education and experience. Up to 1 year of relevant work experience may be required. Preferred Qualifications
Experience working or volunteering directly with patients in a healthcare setting, or with human subjects. Experience with mental health conditions and/or sleep or circadian research. Comfort administering sensitive mental health assessments. CCRC training. Experience with federal regulation adherence. Additional Information
The posting includes standard compensation and benefits information; refer to the official UA job posting for details. The University of Arizona is an equal opportunity employer and a member of the AA/EOE workforce.
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