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Clinical Research Assistant
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- Coordinates and facilitates management of the day-to-day clinical activities for specified research trials in accordance with the research parameters established by the Principle Investigator (PI).
- The Research Assistant (RA) promotes good clinical practices in the conduct of investigations by possessing an in-depth knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection.
- The RA assures compliance with protocol and regulatory requirements, by collecting, recording, and maintaining data and source documentation.
- The RA will work closely with the Clinical Research Staff, department members, study sponsors, and the institution, to support administration of the compliance, personnel and other related aspects of all ongoing clinical studies.
- With program participants; conduct interviews, schedule participant appointments, administer surveys for research purposes, collect and aggregate data, and act as patient liaison for the PI.
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