Senior Medical Writer: Regulatory Clinical Docs

A leading global biopharmaceutical services company is seeking a Senior Medical Writer to develop medical writing deliverables for clinical regulatory submissions. Responsibilities include leading cross-functional teams, preparing regulatory documents, and ensuring compliance with writing standards. The ideal candidate has over 5 years of experience in regulatory writing and expertise in oncology or infectious disease. This role offers flexibility in location across the U.S. or Canada. #J-18808-Ljbffr