Senior Manager, Regulatory Affairs Labeling

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.

Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.

The Opportunity:

The Senior Manager of Labeling serves as a labeling support strategist, partnering with the Global Labeling Lead to execute global labeling deliverables for assigned products. The role develops and maintains regional labeling using the Company Core Data Sheet (CCDS) or an approved reference regional label, adapting content to applicable local requirements while preserving alignment with global labeling strategy. The Senior Manager prepares labeling documents directly or oversees their preparation by external vendors. In both cases, the individual is accountable for document quality, timely delivery, and management of all required cross-functional review and approval activities through completion, in accordance with company procedures and designated approval authorities.

The position can be based at our Redwood City, CA site in a hybrid work schedule (preferred) or remote-based with quarterly and as needed travel.

Labeling Development and Strategic Support

- Partner with the Global Labeling Lead to translate global labeling strategy into actionable regional and country labeling plans, including deliverables, dependencies, timelines, and review requirements.

- Author, revise, and maintain regional prescribing information and patient labeling, as applicable, using the CCDS or an approved reference regional label and relevant supporting documentation

- Assess the impact of CCDS changes, reference label updates, new clinical or safety information, and health authority feedback on assigned labeling; coordinate required updates with regional Regulatory Affairs.

- Identify and document differences between proposed local labeling and the CCDS or reference label. Develop recommendations and coordinate review, escalation, and approval of deviations through established governance processes.

- Responsible for proofreading and departmental QC work; ensure quality of labeling deliverables.

Vendor Oversight

- Define the scope, source documents, content expectations, timelines, and quality standards for outsourced labeling activities; provide clear instructions and ongoing guidance.

- Review vendor-prepared documents for accuracy, completeness, consistency with source labeling, and alignment with applicable requirements. Ensure comments are resolved and deliverables are ready for internal review and approval.

- Monitor vendor performance and escalate quality, resource, or timeline concerns to relevant vendor management stakeholders.

Review and Approval Management

- Own coordination of required reviews and approvals for assigned labeling, regardless of whether documents are authored internally or by a vendor. Identify reviewers and approvers, establish schedules, and manage review and approval workflows through completion.

- Facilitate cross-functional review, consolidate feedback, resolve comments, and drive alignment on proposed content.

- Prepare review materials, document decisions and their rationale, and escalate unresolved content or strategic issues to the Global Labeling Lead.

- Ensure required approvals are obtained and recorded before documents are released for submission or implementation; main