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Qualified Person Responsible for Pharmacovigilance (QPPV) in the EU and UK (homebased)
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About the Role:
- Provide scientific leadership in safety evaluation and risk management for global programs.
- Support regulatory activities and strategic safety decision-making.
Key Responsibilities:
- Lead safety review and risk management for assigned products.
- Evaluate safety data from trials, post-marketing, and literature.
- Support global regulatory submissions and health authority interactions.
Qualifications:
- Advanced scientific or healthcare degree and significant pharmacovigilance experience.
- Experience responding to Health Authority RFIs and strong scientific writing skills.