
Senior Medical Writer/Principal Medical Writer
The role leads development of high-quality, on-time clinical study documents and ensures document management from template to final approved version. Requires a BS (or equivalent) in a scientific/medical discipline, 5+ years' experience as a Senior Medical Writer in sponsor/CRO settings (or 7+ years as Principal), proficiency with Word/Excel/PowerPoint/Adobe/Teams, and knowledge of ICH/FDA/GCP, eCTD, and clinical trial transparency requirements. Oncology and rare disease experience and advanced degrees are listed as preferred.






