Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company is seeking an Associate Director, Regulatory Operations, Europe to support the growing European Regulatory Affairs organization by leading operational planning and execution of regulatory submissions across the region.
Requirements
- Bachelor’s degree in life sciences or related discipline
- 8+ years of experience in regulatory operations, regulatory affairs, or regulatory submission management within the biotechnology or pharmaceutical industry
- Demonstrated experience preparing and publishing eCTD submissions to global health authorities
- Strong understanding of European regulatory submission requirements and procedures
- Hands-on experience using Veeva Vault RIM for regulatory information management
- Hands-on experience using DocuBridge for regulatory publishing
Benefits
- Competitive salary
- Benefits package
- 401k Matching
- Generous Paid Time Off
- Retirement Plan