EU Licensed Pharmacovigilance Specialist

A company is looking for a Freelance/Contract Pharmacovigilance Specialist, Case Processing & QPPV Support. Key Responsibilities Perform end-to-end processing of Individual Case Safety Reports (ICSRs) Assist the QPPV with routine oversight of the Pharmacovigilance system and ensure compliance Support the QPPV in responding to regulatory queries, inspections, and audits Required Qualifications A University degree in a Life-sciences discipline is required Demonstrated experience working in Pharmacovigilance in case processing Ideally skilled in supporting QPPV activities Fluency in English and ideally Swedish (or another EU language) is a must Ability to work hybrid based out of Lund