EU Licensed Pharmacovigilance Specialist

Job Summary

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