Contribute to the development of key study documents in conjunction with Clinical Trial Managers and other functional area leads (e.g., protocols, model informed consent forms, case report forms [CRFs], study manuals, clinical monitoring plans, laboratory manual, pharmacy manual, training materials and site initiation slide presentation). Site management activities, including but not limited to, site training/support, overseeing the timely resolution of data entry queries and missing data, overseeing the timely resolution of site monitoring findings, tracking of enrollment/patient status activities, confirming compliance site informed consent procedures, conduct IP accountability, clinical supplies management, identify and report protocol deviations.