Senior Medical Writer: Regulatory Clinical Docs

A leading biopharmaceutical company is seeking a Senior Medical Writer responsible for developing regulatory documents to support clinical studies. Candidates should have at least 5 years of regulatory writing experience, preferably in oncology or infectious diseases, and should be adept in project management and communication within cross-functional teams. This position allows for remote work from anywhere in the United States or Canada and requires expertise in MS Word as well as a strong understanding of regulatory guidelines. #J-18808-Ljbffr