Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development.

As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: The Manager, Global Regulatory Affairs Project Management is an integral part of the global Regulatory Affairs organization and is responsible for translating complex global regulatory strategies into actionable execution plans, in partnership with and reporting to a Director, Global Regulatory Affairs Project Management. This role applies strong project management expertise and operational leadership to drive cross-functional planning, coordination, and execution of planned and ongoing regulatory activities, across RevMed programs.

The ideal candidate will have a solid understanding of drug development (with oncology experience) and demonstrated hands-on regulatory project management experience supporting early- and/or late-stage development programs, including healthy authority submissions and interactions, in alignment with corporate objectives.

Responsibilities

: Partner with the Director, Global Regulatory Affairs Project Management to lead regulatory submission activities from initiation through submission, defining scope, priorities, timelines, resource

Requirements

, risks, and key deliverables to ensure successful execution. Oversee cross-functional planning and coordination for global regulatory submissions, including INDs, CTAs, NDAs, MAAs, and other major filings, partnering with Regulatory, Medical Writing, Nonclinical, Clinical, Safety, Biostatistics, CMC / Pharmaceutical Development and Manufacturing, etc. and external consultants).

Maintain and communicate integrated submission plans and schedules, proactively tracking progress, identifying risks and dependencies, and implementing mitigation strategies to support on-time regulatory milestones and agency interactions. Partner with Global and Regional Regulatory Science Leads to support the execution of global regulatory strategies for assigned molecules across indications. Facilitate Global Regulatory Teams and meetings to ensure coordinated development and execution of high-quality, timely global regulatory deliverables at the study level.

Propose and support implementation of operational solutions, including process improvements, as appropriate. Partner with the Director, Global Regulatory Affairs Project Management to build and maintain submission dashboards; communicate status, risks, and mitigation strategies to key stakeholders. Support the development, implementation, and continuous improvement of global regulatory project management processes, templates, tools, dashboards, analytics, and best practices.

Champion innovation and operational excellence, identifying opportunities to streamline regulatory project management and enhance submission preparation efficiency and scalability. Required Skills, Experience and Education: Bachelor’s degree in a life sciences or related discipline with 5+ years of pharma / biotech industry experience, including 3+ years of regulatory project management experience. Working knowledge of CTD structure and dossier component management, including coordination across cross-functional filing team contributors and senior leadership.