The Clinical Research Coordinator supports clinical research staff and manages new and ongoing clinical research activities. The role assists clinical investigators and research staff in moving projects forward through close interaction with external clinical research organizations and sponsors. Preparing study documentation—including protocols, amendments, case report forms, serious adverse event reports, and study reports—is an integral part of the job. The coordinator conducts study-related activities in accordance with GCP, ICH, and FDA guidelines. The position coordinates assigned trials, supports research operations, handles regulatory paperwork and study records, and conducts participant screening, scheduling, and protocol-directed visits. It also involves communicating trial status, supporting recruitment and retention, assisting with specimen processing and shipping, and attending required trainings and meetings. The listed pay is $29.95 per hour.
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Job Type
Full-time