Senior Pharmacovigilance Scientist

Location: Welwyn Garden City (Hybrid)
Contract: 12-Month Fixed-Term Contract

We are seeking an experienced Senior Pharmacovigilance Scientist to join a central safety operations team, focused on ensuring high-quality, compliant ICSR processing and safety data management to support patient safety.

Key Responsibilities

• Oversee ICSR case processing and ensure compliance with global regulations
• Manage and monitor service providers, using metrics and performance insights
• Act as a subject matter expert, supporting stakeholders and regulatory inspections
• Drive process improvements and identify/implement CAPAs
• Assess the impact of new or updated regulatory requirements

Experience Required

• Strong background in pharmacovigilance and ICSR processing
• Knowledge of global safety regulations (ICH, EU GVP, FDA)
• Experience in regulatory affairs and vendor oversight
• Proven ability to manage complex projects and influence stakeholders
• Desirable: medical device safety reporting experience

Profile

• Proactive, quality-driven, and solutions-focused
• Strong communicator with the ability to simplify complex topics
• Adaptable, collaborative, and comfortable working in a fast-paced environment

Please follow the link below to apply.