Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The Director of Regulatory Affairs is accountable for the delivery of regulatory strategy for designated programs at RevMed.
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
- Demonstrated success in leading regulatory submissions globally
- Direct experience with oncology drug development
- Excellent communicator
- Excellent planning and organizational skills
- Ability to work simultaneously on multiple projects with tight timelines
Benefits
- Competitive cash compensation
- Robust equity awards
- Strong benefits
- Significant learning and development opportunities