Senior Pharmacovigilance Associate

Job Summary

A company is looking for a Senior Pharmacovigilance Associate III.

Key Responsibilities

• Support the management and maintenance of procedural documents and PSMFs, ensuring compliance with regulatory requirements
• Lead the development of procedural documents across multidisciplinary teams and drive global harmonization of documentation
• Manage the end-to-end process of Global and Local PSMFs, including data collection, quality control, and audit support

Required Qualifications

• Five or more years of experience in pharmacovigilance with a strong understanding of regulatory requirements and processes
• Minimum three years of experience in PV quality management and PSMF maintenance
• Demonstrated experience in implementing cross-functional partnerships and business processes
• Strong command of global pharmacovigilance requirements
• Postgraduate degree required