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Associate Director Global Patient Safety

Job in Camden, Camden County, New Jersey, 08100, USA
Listing for: Regeneron Pharmaceuticals, Inc
Full Time position
Listed on 2026-07-05
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 130000 - 160000 USD Yearly USD 130000.00 160000.00 YEAR
Job Description & How to Apply Below

Build our future together:

At Regeneron, we use science and innovation to develop life‑changing medicines for people with serious diseases. We are seeking an Associate Director, PV Case Operations to join our Global Patient Safety team, supporting case processing across global development and commercial programmes in a hybrid work mode. In this role, you will lead vendor oversight, Individual Case Safety Report (ICSR) quality governance, and inspection readiness while collaborating with vendor teams, internal partners, license partners, auditors, and Health Authority inspectors.

This position offers the opportunity to contribute to a fast‑growing, science‑driven organization making a meaningful difference to patients worldwide.

When & where:

Uxbridge, UK (hybrid)

Discover your role:
  • Own accurate, timely case processing across global development and marketed products, per applicable regulations and Regeneron SOPs.
  • Lead vendor oversight for end‑to‑end ICSR receipt, processing, distribution, and submission.
  • Own ICSR quality standards covering narrative, case validity, and source document reconciliation.
  • Establish tiered quality review frameworks aligned to case complexity, risk, and product lifecycle stage.
  • Monitor submission timelines and vendor SLAs, maintain inspection readiness, and respond to audit findings.
  • Lead root cause analysis and own CAPAs through closure and effectiveness checks.
  • Evaluate AI‑enabled tools for data ingestion, workflow automation, and metrics.
  • You mentor staff and communicate clearly with senior management and partners.
This role requires:
  • Pharmacy, nursing, or equivalent degree required; advanced degree preferred.
  • Typically 10 years of Pharmacovigilance, Drug Safety, or PV Quality experience in pharma or biotech.
  • Well‑informed on FDA, EU, and ICH guidelines governing pharmacovigilance for clinical trial and post‑marketing environments.
  • Experience managing teams on complex, cross‑functional projects.
  • Proven ability to deliver organisational projects through individual contributors or other managers.
  • Strong communication and partner management skills, with ability to resolve and elevate complex issues.
Equal Opportunity – EEO Statement

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Benefits

Regeneron offers a competitive and comprehensive total rewards package including annual bonuses, equity awards, pension or retirement benefits, health and wellness programs, insurance benefits, paid time off, and family support benefits.

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Position Requirements
10+ Years work experience
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