Principal Medical Writer Job at Revolution Medicines 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

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