Lead Site/Study Coordinator

The Lead Site/Study Coordinator supports an assigned group of medical institutions for activities involving clinical trial conduct. They oversee site-level staff tasks, including feasibility assessments, research visits, scheduling, data entry, and monitoring visits. They acts as a constant line of communication between the Milestone One Manager, medical institution staff, and the Sponsor or CRO. They facilitate study evaluations, identify new vendors, and participate in patient recruitment to evaluate for study inclusion. They also perform site quality checks to confirm compliance with protocols. Furthermore, the coordinator assists in developing recruitment tools and training staff, ensuring data accuracy, and supports contract/budget negotiations. They actively participate in study document maintenance and regulatory submissions. The Lead ensures all staff complete necessary training and maintains familiarity with protocols, acting as a resource for Milestone One and site staff. They are responsible for performing tasks within their training and licensure.