Director, Global Regulatory Affairs Project Management

Revolution Medicines is seeking a Director, Global Regulatory Affairs Project Management to join their team. The role will be responsible for translating global regulatory strategies into actionable execution plans and will be a key member of the global Regulatory Affairs organization.

Requirements

• Bachelor’s degree in a life sciences or related discipline; advanced degree preferred.
• 15+ years of pharma / biotech industry experience, including 8-10 years of regulatory project management experience.
• Strong working knowledge of global regulatory regulations, guidelines, and submission pathways.
• Exceptional project management skills with proven ability to manage multiple complex programs under compressed timelines in a fast-paced, cross-functional environment that values both speed and quality.

Benefits

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