Risk Management Pharmacovigilance Specialist

3 weeks ago


Nationwide, United Kingdom SciPro Full time
Join SciPro's Team as a Risk Management Pharmacovigilance Specialist

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.
Requirements:
  • 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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