SciPro 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 role, you will ensure compliance with global PV regulations, lead effective implementation of local and regional RMPs with a critical mindset to continuously improve existing processes, whilst contributing to the development of new procedures in close collaboration with global stakeholders.

Key responsibilities:

• Support the finalization of RMPs and RMMs including relevant material.
• 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.

Key Requirements:

• Knowledge of worldwide RMP regulations: prior experience with European Union (EU) regulations is 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.