Qualified Person for Pharmacovigilance

The Qualified Person for Pharmacovigilance (QPPV) is responsible for establishing and maintaining a compliant European pharmacovigilance system to support clinical development, regulatory submissions, and future commercialization. This role ensures adherence to EMA Good Pharmacovigilance Practices (GVP), manages safety reporting processes, and partners with cross-functional teams to integrate patient safety throughout the product lifecycle. The position involves developing scalable pharmacovigilance capabilities and providing expert guidance on European safety requirements.