Freelance QPPV (EU and UK). Various EU Locations Considered.
ClinigenIreland • West Lancashire, England, United Kingdom
Posted March 10, 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 qualified personnel for Pharmacovigilance (QPPV) to support the delivery of specialist pharmaceuticals and services globally. This flexible role involves serving as the EU and UK QPPV, ensuring compliance with regulations, managing safety reports, and working closely with cross-functional teams. The role is on a contract basis with ongoing projects.
Requirements
- Act as a Qualified Person for Pharmacovigilance and/or Local Contact Person for PV in the EU and UK
- Oversee pharmacovigilance activities and ensure compliance with EU and UK legislation
- Manage and implement pharmacovigilance systems, including safety databases and processes.
- Work with regulatory affairs, medical, and clinical operations to ensure compliance.
- Provide guidance on safety-related matters for clinical trials and post-marketing settings.
