Supervisory Clinical Research Protocol

Advise prospective investigators on ethical, technical and procedural requirements for protocol development. Oversee the arrangements and coordination for Committee meetings and ensures all committee members receive all the required documents for review. Obtain, process, and document adverse events, amendments, protocol deviations, and timely literature searches. Serve as a backup Recorder and a non-voting member of the Institutional Review Board (IRB) during the absence of the IRB Manager at convened meetings. Ensure all protocols submitted are reviewed to assure the researcher has complied with regulations pertaining to the administrative conduct of research. Provide and identify needed development and training.