Director, Regulatory Affairs Labeling

Role: Director, Regulatory Affairs Labeling at Revolution Medicines, leading global regulatory labeling strategies for pipeline, late-stage, and marketed oncology products, with a focus on RAS-targeted therapies. Responsibilities include developing, reviewing, and approving labeling documents (Target, Core, Regional), managing cross-functional Labeling Working Group and senior committees, staying current with labeling regulations, and liaising with global authorities. The role involves strategic guidance on labeling content, negotiating updates, and ensuring compliance across regions. Requirements: Bachelor's in science or related field, 12+ years in biotech/pharma with extensive experience in product labeling across multiple regions, strong regulatory review skills, and leadership in cross-functional meetings. Preferred: Advanced degree and 10+ years relevant experience. High-Value: Oncology, RAS inhibitors, late-stage clinical development, global regulatory interactions, and labeling compliance. WorkSetup: Hybrid at Redwood City, CA, or remote with quarterly travel.