Risk Management Pharmacovigilance Specialist
3 weeks ago
We are seeking a highly skilled Risk Management Pharmacovigilance Specialist to join our team at SciPro, a leading global pharmaceutical company. As a Risk Management Pharmacovigilance Specialist, you will play a critical role in supporting the QPPV office and DSPV functions on the oversight and finalization of RMP and RMMs as a subject matter expert within the EMEA PV team.
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 and oversight of RMP commitments.
- Support QPPV team in strategic impact assessment of PV regulations intelligence items.
- Knowledge of worldwide RMP regulations, with prior experience with European Union (EU) regulations required.
- Exposure to working relationships with regulatory authorities.
- Demonstrable, hands-on experience of implementing local and regional RMPs.
- Ability to independently lead long- and short-term project timelines and deliverables.
As a Risk Management Pharmacovigilance Specialist, you will have the opportunity to work closely with global stakeholders to develop new procedures and continuously improve existing processes. If you are a motivated and experienced professional with a passion for pharmacovigilance and risk management, we encourage you to apply for this exciting opportunity.
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Risk Management Pharmacovigilance Specialist
1 month ago
Nationwide, United Kingdom SciPro Full timeSciPro is partnering with a leading global pharmaceutical company to find a skilled Risk Management Pharmacovigilance Specialist.This role supports the QPPV office and DSPV functions in overseeing and finalizing RMP and RMMs as a subject matter expert within the EMEA PV team.Key responsibilities include ensuring compliance with global PV regulations,...
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Risk Management Pharmacovigilance Specialist
1 month ago
Nationwide, United Kingdom SciPro Full timeSciPro is partnering with a leading global pharmaceutical company to find a skilled Risk Management Pharmacovigilance Specialist.This role supports the QPPV office and DSPV functions in overseeing and finalizing RMP and RMMs as a subject matter expert within the EMEA PV team.Key responsibilities include ensuring compliance with global PV regulations,...
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Risk Management Pharmacovigilance Specialist
1 month ago
Nationwide, United Kingdom SciPro Full timeSciPro are exclusively partnered with a leading, global pharmaceutical company with a culture of patient centricity, supporting their search for a Risk Management Pharmacovigilance Specialist. This role supports the QPPV office and DSPV functions on the oversight and finalization of RMP and RMMs as a subject matter expert within the EMEA PV team. Within the...
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