Director, Regulatory Affairs

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company is seeking a Director, Regulatory Affairs to provide clear, effective regulatory strategy as the Regulatory Study Lead for global oncology programs.

Requirements

• Degree in life sciences, pharmacy, medicine, or related fields
• Minimum 12 years in the pharmaceutical/biotech industry or relevant work experience
• Minimum 8 years in Regulatory Affairs including regulatory strategy and leadership roles
• Proven success in developing and delivering global regulatory strategies and submissions
• Previous experience with NDA and/or global marketing application filings
• Previous experience with global ODD annual reports
• Demonstrated success in leading health authority interactions and negotiations
• Direct experience in oncology drug development including oversight of large, global Phase 3 studies
• Skilled at representing Regulatory on cross-functional teams and presenting to senior leadership
• Excellent communication, planning, and organizational skills with the ability to manage multiple projects and tight deadlines

Benefits

• Competitive cash compensation
• Robust equity awards
• Strong benefits
• Significant learning and development opportunities