TMF & Document Management Lead - Associate Director

A global commercial-stage pharmaceutical company is seeking an Associate Director, Document Management and Trial Master File. This role involves providing strategic leadership in managing GxP documents, ensuring team oversight, driving process improvements, and serving as a subject matter expert. The ideal candidate will have substantial experience in TMF management and a strong knowledge of regulatory requirements. This position offers a dynamic work environment where one can contribute significantly to clinical programs and their compliance. #J-18808-Ljbffr