Senior Medical Writer | Regulatory Lead, Cross‑Functional

A leading global biopharmaceutical services company is seeking a Senior Medical Writer. This role involves developing medical writing deliverables for clinical regulatory submissions. Ideal candidates will have a minimum of 5 years' experience in writing regulatory documents, preferably in oncology or infectious diseases, and strong communication skills. Responsibilities include leading cross-functional teams, authoring clinical documents, and ensuring compliance with regulatory standards. The position is open to candidates located anywhere in the United States or Canada. #J-18808-Ljbffr