- Location
- Cambridge, MA
- Workplace
- Remote
- Type
- Full-time
- Department
- Regulatory
- Seniority
- Senior
- Source
- Lever
Description
Summary
The Senior Director, Regulatory Affairs leads and coordinates regulatory interactions and submission execution for ARTBIO’s clinical-stage radiopharmaceutical programs. This role is primarily responsible for coordinating regulatory medical writing across functions. The position works cross-functionally to translate research and development data and strategy into clear, compliant regulatory communications and high-quality submission deliverables.
Skills
FDACompliance
Benefits
A unique chance to contribute to first-in-class cancer therapies.Exposure to both radiochemistry and CMC development in a dynamic biotech setting.Hands-on training and professional development opportunities.An international, collaborative, and supportive work culture.Competitive compensation and benefits.