Job Description
Responsibilities
- Provide proactive, strategic legal advice to RayzeBio leadership and cross‑functional teams (R&D, regulatory, medical, manufacturing, quality, supply chain, commercial).
- Advise on global radiopharmaceutical regulatory matters, including FDA drug development, clinical trials, approval, labeling, advertising/promotion, and cGMP.
- Advise on handling, transport, and disposal of radioactive materials (NRC, DOT, and other applicable regulations).
- Draft, review, and negotiate clinical trial, supply, manufacturing, licensing, collaboration, and research agreements.
- Monitor global legal/regulatory/enforcement developments and advise on emerging risks and compliance strategies.
- Partner with BMS Legal and Compliance to align with company standards, global frameworks, and best practices.
Qualifications & Experience
- J.D. required; admitted to practice law in at least one U.S. jurisdiction. <...
Ready to Apply?
Submit your application today and join our talented team at Scorpion Therapeutics.
Submit ApplicationJob Details
- Location san diego, laguna
- Job Type Full-time
- Category Other
- Posted Date June 09, 2026
- Application Deadline July 19, 2026