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Risk Management Pharmacovigilance Specialist
2 months ago
SciPro is seeking a highly skilled Risk Management Pharmacovigilance Specialist to join our team. As a subject matter expert, you will play a critical role in supporting the QPPV office and DSPV functions in the oversight and finalization of RMP and RMMs.
Key Responsibilities:- Support the finalization of RMPs and RMMs, including relevant materials.
- Assist Medical Safety leadership and MSLs with compliance oversight and tracking tool planning.
- Support QPPV team in strategic impact assessment of PV regulations intelligence items.
- Knowledge of worldwide RMP regulations, with prior experience in European Union (EU) regulations.
- Exposure to working relationships with regulatory authorities.
- Demonstrable hands-on experience in implementing local and regional RMPs.
- Ability to lead long- and short-term project timelines and deliverables.
As a Risk Management Pharmacovigilance Specialist, you will be responsible for ensuring compliance with global PV regulations and leading the implementation of local and regional RMPs. If you have a strong background in pharmacovigilance and risk management, and are looking for a challenging role, please apply.