Freelance QPPV (EU and UK). Various EU Locations Considered.
ClinigenNetherlands
Posted September 26, 2025
Contract / Temporary
About the Company
Our mission is to accelerate access to medicines for patients in every corner of the globe: Clinical Services, Product Access and Commercialisation, Pharmacovigilance and Regulatory Affairs.
Job Description
Clinigen is seeking a freelance Qualified Person for Pharmacovigilance (QPPV) for the EU and UK to provide support for various clients. This role involves managing pharmacovigilance activities, ensuring compliance with regulations, and maintaining a pharmacovigilance system. The position offers flexibility based on workload.
Requirements
- Experience in acting as a QPPV
- Expert knowledge of PV legislation in EU and UK
- Minimum of 7 years' demonstrated experience in managing or implementing PV systems
- Extensive knowledge of global pharmacovigilance regulations and GVP and GCP guidelines
- Experience in pharmacovigilance safety risk management
- Experience in participation in audits and Regulatory authority inspections
- Life Science Degree
