Pharmacovigilance Case Processing Lead

Are you a Pharmacovigilance professional with 4 years or more experience in PV Case Processing looking to join a global, innovation-driven pharmaceutical organisation with a growing pipeline?

We have been retained by a highly respected global pharmaceutical company in the search for 3 PV Case Processing Leads to join their Global Safety team based in the Paris.

What you'll be doing:

• Vendor management of outsourced case processing activities from intake through regulatory submission for both Clinical and Post market cases
• Quality review of vendor-managed IC…
• Investigation of deviations, root cause analysis and CAPA management
• Supporting clinical trials through Safety Management Plans and safety system configuration
• Vendor management, reconciliation activities and operational oversight
• Acting as a Subject Matter Expert during audits and inspections

What we're looking for:

• 4+ years' Pharmacovigilance Case Processing experience (Global)
• Strong knowledge of global PV regulations and ICSR requirements
• 1+ year experience working with ARGUS (recent)
• 2 years vendor oversight and quality management experience
• Comfortable working in an international, cross-functional environment

Why consider this opportunity?

• Join a company investing heavily in R&D and future innovation
• Exposure across both clinical and post-marketing safety activities
• High visibility role with significant vendor and stakeholder interaction
• Opportunity to contribute to process improvement and operational excellence
• Collaborative international environment with strong long-term growth plans

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