📍 Location: London (West Works), United Kingdom
📁 Department: Patient Safety & Pharmacovigilance, Development
👤 Reports to: Patient Safety Group Manager

🚫 Please Note:

Relocation support is not available for this position. Candidates must already be based in the United Kingdom and have existing work authorization.

🔍 What You’ll Do

• Lead the collection, documentation, and reporting of adverse events across clinical trials, patient programs, literature, and spontaneous reports.
• Coordinate safety submissions (SAE, SUSAR, DSUR) to Local Health Authorities and internal stakeholders.
• Collaborate with global and local Patient Safety teams to ensure accurate safety data evaluation.
• Monitor national pharmacovigilance regulations and update global teams accordingly.
• Perform reconciliation with other departments for potential AEs
• Support audits, inspections, and corrective action plans with precision and professionalism.
• Maintain electronic filing and archiving systems for safety documentation.

🎯 What Success Looks Like

• Timely and high-quality safety reporting and KPI submissions.
• Zero critical findings in audits or inspections.
• Positive feedback from internal and external stakeholders.

🎓 Your Background

• Degree in Life Sciences or Health Care Sciences (or equivalent).
• Fluent in written and spoken English.
• Strong knowledge of pharmacovigilance regulations and medical terminology.
• Experience with Argus safety database is a plus.
• Excellent communication, negotiation, and interpersonal skills.
• Tech-savvy and quality-focused.