Local Qualified Person for Pharmacovigilance

Responsibilities

• Maintain the local pharmacovigilance system in compliance with local legislation and Good Pharmacovigilance Practices (GVPs)
• Manage the development, negotiation, and execution of safety agreements for large, complex projects
• Act as the primary point of contact or deputy for assigned projects and manage customer relationships
• Prepare, maintain, and review Pharmacovigilance System Master Files (PSMFs) and Pharmacovigilance System Descriptions (PSSFs)
• Customize project documentation to accurately reflect services provided and oversee final distribution
• Provide advice, support, and guidance to other staff members and project teams

Requirements

• Bachelor's Degree in health science
• 2 years of experience in a Contract Research Organization (CRO) or Pharmaceutical company
• At least 1 year of Lifecycle Safety experience (including PSMF/PSSF management, PVA, or Aggregate reporting)
• Excellent knowledge of Lifecycle Safety processes and local pharmacovigilance regulations
• Strong written and verbal communication skills with high attention to detail
• Ability to manage multiple projects simultaneously and organize competing priorities

About the Company

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.