Per Diem Clinical Research Coordinator - Rehabilitation and Human Performance

Job description

The Per Diem Clinical Research Coordinator performs all the regular duties of a full or part time Clinical Research Coordinator, but on an as-needed basis. In addition, due to a limited number of hours, does not apply for Exempt status as is normal in this group. This individual assists in activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information, and may perform phlebotomy duties. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office). Non-Bargaining Unit, 857 - Rehabilitation and Human Performance - ISM, Icahn School of Medicine - Collates and tabulates research data. - Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements. - Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires. - Assists in preparing grant applications, IRB/GCO for submission and filings. - Maintains source documents and subject...