**This is a flexible position after probationary period.**The Protocol Project Manager will provide support, coordination, and leadership for FDA-regulated studies which may involve industry-sponsored Phase I, II, III, and IV clinical trials, government-funded clinical research, and investigator-initiated clinical research (collectively referred to as "clinical research involving human subjects"). Ensure smooth, accurate progress of clinical studies from the planning and approval stages through study completion and post-study closure. Prepare documentation for submission for review by the Institutional Review Board (IRB), recruit and screen study participants, coordinate their clinical treatment and follow-up care, and help facilitate their co