Scientific Writer, Integrated Research Management

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The companys 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:

We are seeking a Scientific Writer with strong nonclinical regulatory experience to support the authoring and integration of nonclinical content for U.S. and global regulatory submissions. This role focuses on developing and integrating nonclinical content beyond INDs and NDAs including briefing documents Investigator Brochures responses to health authority questions and other submission-related materials across the U.S. Europe and Asia.

As a strategic scientific integrator this individual will translate complex RAS biology and translational pharmacology into clear compelling regulatory narratives that reflect RevMeds deep mechanistic understanding of RAS signaling and frontier targets. The role partners closely with nonclinical subject matter experts (SMEs) in pharmacology toxicology and DMPK as well as Regulatory Affairs Regulatory Operations and Medical Writers to ensure nonclinical strategy and content are scientifically rigorous aligned and submission-ready.

The Scientific Writer will leverage structured source documents document management systems and emerging AI-enabled tools to improve efficiency consistency and scalability of nonclinical regulatory writing. This role requires strong organizational skills and the ability to manage multiple programs and cross-functional inputs simultaneously in a fast-paced scientifically rigorous environment.

Key Responsibilities

• Author integrate and edit nonclinical sections of regulatory documents across multiple submission types including INDs NDAs briefing documents amendments and response to health authority requests.

• Safeguard and articulate the scientific rationale underlying RevMeds RAS(ON) and companion inhibitor programs across regulatory communications.

• Develop clear hypothesis-driven regulatory narratives that integrate pharmacology toxicology and DMPK data and engage as a critical scientific thought partner to these functions to strengthen mechanistic coherence regulatory positioning and alignment with global regulatory expectations (FDA EMA and select Asian agencies).

• Collaborate closely with project Medical Writers to ensure nonclinical sections are delivered in alignment with overall timelines and coordinated with related document sections.

• Ensure scientific consistency across programs to preserve and extend RevMeds reputation for rigor and mechanistic depth.

• Manage multiple regulatory writing efforts in parallel balancing priorities across programs and functions in a fast-paced environment.

• Utilize Regulatory information management systems (e.g. Veeva) and AI-enabled writing tools to support authoring review and lifecycle management of regulatory documents.

• Contribute to templates guidance and best practices for global nonclinical regulatory documentation.

• Drive continuous improvement of nonclinical authoring standards templates and knowledge management systems.

• Capture and institutionalize lessons learned from prior submissions to improve quality consistency and efficiency across programs and regions.

Required Skills Experience and Education:

• Advanced degree (PhD preferred; MS considered) in a relevant nonclinical scientific discipline.

• Demonstrated experience authoring or substantially contributing to nonclinical sections of regulatory submissions across multiple document types.

• Strong working knowledge of pharmacology toxicology and DMPK and their integration into regulatory narratives.

• Demonstrated ability to synthesize complex mechanistic datasets into coherent hypothesis-driven regulatory narratives.

• Comfortable engaging deeply in data discussions with subject matter experts and operating in a culture of scientific debate and rigorous review.

• Familiarity with range of regulatory expectations including those beyond the U.S. such as European and/or Asian health authorities.

• Proven ability to manage multiple projects concurrently and work effectively across functions.

• Excellent written communication skills attention to detail and a collaborative solutions-oriented mindset.

Preferred Skills:

• Industry experience as a Scientific or Medical Writer.

• Experience supporting global regulatory submissions (FDA EMA etc.).

• Proficiency with Veeva or similar Regulatory information management systems platforms.

• Experience leveraging AI-enabled tools for scientific or regulatory writing.

• Comfortable operating in a dynamic evolving research and development environment. #LI-Hybrid #LI-LN1