Supervises staff involved in routine research study coordination. Receives predetermined work assignments that are subject to a moderate level of control and review. Oversees staff in the execution of assignments; trains and mentors staff to improve the quality and quantity of work.Manages applications to the Food and Drug Administration (FDA), Research Advisory Panel of California (RAPC), and Institutional Review Board (IRB).Coordinates Schedule 1 DEA licensure; the handling, storage, and accountability documentation of Schedule 1 investigational products; and coordination with pharmaceutical manufacturers for investigator-initiated trials.Engage with the Office of Clinical Trial Activation (OCTA), Clinical Research Services (CRS), BearBuy, and other uni