• Monitor clinical trial programs and manage regional clinical trial sites. • Collaborate with an assigned clinical research team to provide input on site selection, study initiation procedures, conflict resolution, and audit responses. • Conduct or assist with site evaluations, study initiations, routine monitoring, site close-outs, and FDA audit preparations. • Effectively communicate all relevant findings with appropriate in-house personnel. • Develop territory to broaden selection of research study sites. • Manage work activities in a time and cost-effective manner to ensure budgetary guidelines and project timelines are met. • Participate in internal and/or external meetings to maintain current knowledge on regulations and guidelines.