TMF & Document Management Lead - Associate Director

A leading pharmaceutical firm is seeking an Associate Director for Document Management and Trial Master File (TMF) in Newton, MA. This role involves strategic oversight of GxP Document management across clinical programs, ensuring TMFs are complete, accurate, and compliant. The ideal candidate will have expertise in TMF operations, strong leadership capabilities, and experience with regulatory inspections. This is an opportunity to contribute to clinical excellence in a dynamic environment. #J-18808-Ljbffr