Global Patient Safety: Associate Director (Hybrid)

Regeneron UK Limited; Uxbridge; Hybrid; GBP 90.000 - 130.000; Vollzeit

Benefits dieser Stelle

Annual bonuses

Pension benefits

Health programs

Paid time off

Zusammenfassung

Regeneron seeks an Associate Director to lead pharmacovigilance case operations in a hybrid setting. You will oversee ICSR receipt, processing, distribution and submission across global development and commercial programmes, while managing vendors and ensuring quality standards and inspection readiness.

You will tailor reviews by complexity and lifecycle stage, optimise AI-enabled data ingestion and workflows, and mentor staff.

Qualifikationen

• Pharmacy, nursing or equivalent qualification.
• Experience in pharmacovigilance, drug safety or pharmacovigilance quality experience, typically 10 years.
• Knowledge of FDA, EU and ICH pharmacovigilance requirements across clinical trials and post‑marketing.
• Experience supervising teams on complex projects and cross‑functional collaboration.

Aufgaben

• Oversee timely ICSR receipt, processing, distribution and submission across global portfolios.
• Maintain vendor resourcing, training, volume readiness and structured feedback.
• Lead corrective and preventive actions and root cause analysis for recurring issues.

Kenntnisse

Team leadership

Cross-functional collaboration

Project management

Vendor governance

Ausbildung

Pharmacy, nursing or equivalent qualification

Advanced degree preferred

Jobbeschreibung

Regeneron seeks an Associate Director to lead pharmacovigilance case operations in a hybrid setting. You will oversee ICSR receipt, processing, distribution and submission across global development and commercial programmes, while managing vendors and ensuring quality standards and inspection readiness.

You will tailor reviews by complexity and lifecycle stage, optimise AI-enabled data ingestion and workflows, and mentor staff.