Scientific Writer, Integrated Research Management

Revolution Medicines

Redwood City, United States
Base: $143,000—$178,000 usd; bonus/equity: not spe...
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Nonclinical regulatory submissions
Ras biology and translational pharmacology
Authoring and integration of nonclinical content
** Revolution Medicines is seeking a Scientific Writer with a strong background in nonclinical regulatory submissions to support their oncology-focused R&D efforts. The ideal candidate will have expertise in pharmacology, toxicology, and DMPK, and the ability to create compelling regulatory narratives for various submission types. **

Job Summary

  • Support the authoring and integration of nonclinical content for U.S. and global regulatory submissions, focusing on documents beyond INDs and NDAs.
  • Translate complex RAS biology and translational pharmacology into clear, compelling regulatory narratives, partnering closely with nonclinical SMEs and Regulatory Affairs.
  • Leverage structured source documents, document management systems, and emerging AI-enabled tools to improve efficiency, consistency, and scalability of nonclinical regulatory writing.

Matching Summary

Match Score: 75

** Revolution Medicines is seeking a Scientific Writer with a strong background in nonclinical regulatory submissions to support their oncology-focused R&D efforts. The ideal candidate will have expertise in pharmacology, toxicology, and DMPK, and the ability to create compelling regulatory narratives for various submission types. **

Salary

Base: $143,000—$178,000 USD; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • nonclinical regulatory submissions
  • RAS biology and translational pharmacology
  • authoring and integration of nonclinical content
  • U.S. and global regulatory submissions
  • pharmacology, toxicology, and DMPK integration

Nice-to-have

  • AI-enabled writing tools
  • scientific debate and rigorous review
  • dynamic, evolving research and development environment

Key Requirements

  • Advanced degree (PhD preferred; MS considered)
  • Demonstrated experience authoring nonclinical regulatory submissions
  • Familiarity with FDA, EMA, and select Asian agencies

Work Rights

Not specified

Tailored Resume

Cover Letter