Principal Medical Writer
Revolution Medicines · Remote
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Revolution Medicines seeks a Principal Medical Writer with 8-11 years of clinical regulatory writing experience to lead preparation of submission-ready documents for oncology drug development programs. This individual contributor role includes team leadership responsibilities and requires expertise in clinical regulatory submissions.
What they're looking for
- 8-11 years clinical regulatory writing experience in biopharmaceutical companies
- Prior BLA/NDA/MAA medical writing experience
- Advanced degree in clinical/life sciences, English, journalism, or communications
- Proficiency in Microsoft Word including styles and templates
- Familiarity with AMA style guidelines
- Ability to manage competing deadlines and foster cross-functional collaboration
What you'll be doing
- Lead medical writing on complex clinical regulatory documents including protocols, IBs, CSRs, and NDA modules
- Serve as primary medical writing contact for one or more clinical development programs
- Develop and maintain document templates, processes, and medical writer onboarding materials
- Schedule document reviews, manage adjudication meetings, and mentor junior and contract writers
- Identify scheduling and resource conflicts across projects and recommend resolutions
Privacy & handoff
This role links to Revolution Medicines's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.