The OCR Clinical Research Monitor completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial research both from a documentation and process level. Monitors all extramural research program investigator initiated studies being conducted at FCCC and other academic institutions. Ensures protocol compliance at the clinical research sites. Other applicable certification may be considered in lieu of those listed below (i.e. Regulatory Affairs).
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Career Level
Mid Level