Pharmacovigilance Scientist Freelance

The role

Working within the drug safety function, you'll take ownership of day-to-day PV deliverables, from individual case management through to aggregate reporting and signal work, helping keep the client's safety operations compliant and inspection-ready during a busy period.

Key responsibilities

• End-to-end ICSR processing, case intake, triage, data entry, medical assessment support, narrative writing and quality review, within agreed timelines
• Contributing to aggregate safety reports (PSURs/PBRERs, DSURs, addendum reports) and supporting the wider periodic reporting cycle
• Supporting signal detection, evaluation and tracking, and helping maintain safety data quality
• Scientific and medical literature screening for adverse events and safety information
• Expedited and periodic regulatory reporting in line with EU/global requirements
• Maintaining compliance with SOPs, safety agreements (SDEAs) and applicable regulations, and supporting audit and inspection readiness

What we're looking for

• Solid pharmacovigilance experience (5+ years) in a pharma, biotech or CRO setting (clinical and/or post-marketing)
• A life-sciences, pharmacy, nursing or related degree (or equivalent experience)
• Hands-on with a validated safety database, [Argus / ARISg / Veeva]
• Strong working knowledge of EU and ICH pharmacovigilance requirements (GVP modules, E2B, expedited/periodic reporting)
• Excellent written English, attention to detail, and the ability to work independently at pace
• Available immediately (or at short notice) to commit to the contract term