Senior Manager, Global Pharmacovigilance Operations

Bristol-Myers Squibb Co; Princeton (NJ); On-site; USD 150,000 - 182,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid holidays

Vacation time

Stock opportunities

Wellbeing support

Insurance

Job summary

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks a senior leader to oversee Global Patient Safety case management and PV operations. You will manage external vendors, ensure regulatory compliance, and drive risk management initiatives across the PV function.

Join a multidisciplinary team in Princeton, NJ, contributing to safety submissions, inspections readiness, and cross-functional collaboration with clinical and quality groups.

Qualifications

• BS/BA degree in related discipline; 10 years of related experience or equivalent combination.
• 8+ years in Drug Safety and Pharmacovigilance, PV operations.
• Working knowledge of international regulatory Adverse Event reporting requirements.
• Experience guiding PV vendor staff.
• Strong knowledge of US and international regulations for clinical trial and post-marketing safety.

Responsibilities

• Lead global ICSR activities to comply with ICSR regulations.
• Oversee PV operations programs and vendor compliance.
• Support inspection readiness and data outputs for safety reports.
• Collaborate with stakeholders to ensure PV compliance and risk management.

Skills

Global PV operations

Regulatory knowledge (US/intl)

Vendor management

Cross-functional collaboration

Leadership/mentoring

Education

Bachelor's degree in related discipline

Job description

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks a senior leader to oversee Global Patient Safety case management and PV operations. You will manage external vendors, ensure regulatory compliance, and drive risk management initiatives across the PV function.

Join a multidisciplinary team in Princeton, NJ, contributing to safety submissions, inspections readiness, and cross-functional collaboration with clinical and quality groups.