The Clinical Research Coordinator II provides assistance on clinical research studies in Preventive Medicine, following established policies, procedures, and study protocols. The role supports participant recruitment, evaluation, and consent; patient data collection and organization; study-visit scheduling; clinical tests such as phlebotomy and EKGs; and maintenance and updating of study data. The position also supports sponsor and organizational compliance, study documentation, regulatory submissions, and quality assurance and quality control procedures. Patient care is not required for this position. Candidates completing a bachelor's degree may provide degree-equivalency verification within six months of hire, or within one year if starting on a per-diem basis. The role is based at 399 Revolution Drive and is hybrid, with 40 scheduled hours per week on the day shift.
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Job Type
Full-time
Career Level
Mid Level