Revolution Medicines is hiring: Principal Medical Writer in Redwood City

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionariesin a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

Revolution Medicines is seeking a motivated individual with a clinical regulatory writing background to play a critical role in the successful preparation of high-quality, submission-ready clinical research documents. This role is an individual contributor with team leadership responsibilities, reporting into the Executive Director, Medical Writing.

• Serves as medical writing lead on complex clinical regulatory documents, including protocols, IBs, CSRs, briefing documents, periodic safety reports, risk management documents, and IND and NDA modules.

• Assists in developing and maintaining document templates, department standard processes and work instructions, medical writer onboarding materials, and style guide.

• Serves as primary medical writing contact for one or more clinical development programs.

• Represents medical writing at cross-functional planning meetings.

• Effectively communicates deliverables needed, the writing process, and timelines to team members.

• Schedules document reviews and manages adjudication meetings.

• Holds team members accountable to agreed-upon project dates.

• Independently resolves document content issues and questions.

• Ensures consistency, clarity, and accuracy both within and across documents.

• Recognizes potential scheduling and resource conflicts across projects and provides recommendations to resolve.

• Mentors junior and contract medical writers on both document and timeline management.

Required Experience, Skills, and Education:

• 8+ years of clinical regulatory writing experience within one or more biopharmaceutical companies, including prior experience working as a medical writing for a BLA/NDA/MAA.

• Advanced degree in clinical or life sciences, English, journalism, and/or communications.

• Proficiency in Microsoft Word, including the use of MS Word styles and templates.

• Familiarity with AMA style.

• Ability to successfully manage and prioritize writing projects with competing deadlines, to foster collaborative cross-functional relationships, and to drive high-quality regulatory writing projects to successful submission.

• Ability to work in a high-pressure environment with short deadlines while remaining calm, focused, professional, diplomatic, and positive.

Preferred Skills:

• Experience with oncology therapeutics.

• Familiarity with PleaseReview, StartingPoint, EndNote, and Smartsheet.

• Experience performing QC reviews of clinical regulatory documents. #LI-Hybrid #LI-YG1