Senior Director, Global Safety & PV – Oncology

Bristol-Myers Squibb; Princeton (NJ); On-site; USD 307,000 - 372,000; Full time

Benefits offered by this job

Health coverage

Wellbeing programs

Financial planning benefits

Paid time off

Job summary

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks a Safety Medical Doctor to lead global pharmacovigilance strategies and proactive safety surveillance across clinical development and post-marketing programs. You will partner with clinical, regulatory, and safety teams to ensure robust risk management and regulatory compliance.

The role requires an MD with 10+ years in PV, strong leadership, and ability to mentor cross-functional teams while driving safety science excellence and

Qualifications

• MD or equivalent with 10+ years pharmacovigilance/safety experience.
• Experience with global pharmacovigilance regulations (FDA, EMA, ICH).
• Proven expertise in signal detection, risk management, and aggregate safety reporting.
• Experience interacting with global regulators and scientific advisory bodies.

Responsibilities

• Lead or co-lead global pharmacovigilance strategy and proactive safety surveillance.
• Establish safety governance structures, SOPs, and continuous improvement processes.
• Collaborate with safety, clinical, regulatory, and medical affairs teams to integrate safety insights.
• Direct safety evaluation and benefit-risk assessment for trials and post-marketing products.
• Represent Safety Science in safety management teams and regulatory interactions.
• Produce safety content for protocols, DSURs, PSURs, RMPs, and regulatory responses.
• Mentor cross-functional colleagues on PV concepts and practices.
• Leverage AI to improve safety program performance and decision making.

Skills

Leadership

Communication

Matrixed environment

Patient safety ethics

Travel willingness

Education

MD or equivalent

Job description

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks a Safety Medical Doctor to lead global pharmacovigilance strategies and proactive safety surveillance across clinical development and post-marketing programs. You will partner with clinical, regulatory, and safety teams to ensure robust risk management and regulatory compliance.

The role requires an MD with 10+ years in PV, strong leadership, and ability to mentor cross-functional teams while driving safety science excellence and