Senior Medical Writer: Regulatory Clinical Docs Job at Parexel in Baton Rouge

A leading biopharmaceutical consulting firm is seeking a Senior Medical Writer to develop medical writing deliverables supporting clinical regulatory portfolios. The ideal candidate will lead cross-functional teams, manage timelines, and must have a minimum of 5 years in writing regulatory documents, particularly in oncology or vaccines. Excellent communication skills and fluency in American English are essential for this remote position. #J-18808-Ljbffr