Associate Director, Regulatory Affairs CMC
Olema OncologyBoston, Massachusetts, United States • San Francisco, California, United States
Posted March 29, 2026
190000 - 220000 USD
Full Time
About the Company
No company description available.
Job Description
Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. The Associate Director, Regulatory Affairs CMC, will be responsible for developing and executing the CMC regulatory strategies for Olema product(s) in development and post-approval.
Requirements
- Bachelor's degree in a scientific field
- Excellent knowledge of current CMC regulations and regulatory procedures
- Minimum 8 years of experience working in clinical research, biotech, and/or pharmaceutical company
- Experience in small molecule drug development
- Global CMC regulatory experience for clinical trials
- Post approval (commercial) experience is a plus
Benefits
- Competitive compensation and benefits package
- Equity
- Bonus
- Flexible and friendly work environment
- Open communication and collaborative team culture