Senior Counsel, RayzeBio
Bristol Myers Squibb
5 months ago
Remote friendly (San Diego, CA)
United States
Corporate Functions
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.
- 8–12+ years legal experience in biotech/pharma/life sciences with significant FDA regulatory and healthcare law counseling.
- Strongly preferred: oncology, radiopharmaceuticals, or complex therapeutic modality experience.
- Business-oriented legal judgment; strong interpersonal skills; risk assessment and strategic thinking; effective in multidisciplinary, cross-functional teams.
Benefits (as listed):
- Health coverage (medical, pharmacy, dental, vision); wellbeing programs; 401(k); disability and life insurance; paid time off (flexible time off/paid vacation per employee category).
Compensation (as listed):
- San Diego, CA: $243,470–$295,033.
- 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.
- 8–12+ years legal experience in biotech/pharma/life sciences with significant FDA regulatory and healthcare law counseling.
- Strongly preferred: oncology, radiopharmaceuticals, or complex therapeutic modality experience.
- Business-oriented legal judgment; strong interpersonal skills; risk assessment and strategic thinking; effective in multidisciplinary, cross-functional teams.
Benefits (as listed):
- Health coverage (medical, pharmacy, dental, vision); wellbeing programs; 401(k); disability and life insurance; paid time off (flexible time off/paid vacation per employee category).
Compensation (as listed):
- San Diego, CA: $243,470–$295,033.