Coordinates and supports Site Qualification Visits (SQVs), Site Initiation Visits (SIVs), routine monitoring visits, audit visits, and study closeout visits, including scheduling, preparation of required documentation, meeting coordination, facility tours, and follow-up of action items. Serves as a primary point of contact for study-related communications with Principal Investigators, Sub-Investigators, sponsors, Contract Research Organizations (CROs), vendors, laboratory personnel, pharmacy, nursing, and other internal and external stakeholders.