Requirements & Experience:

• Process and assess adverse event reports in line with EU GVP requirements
• Perform data entry and quality checks on ICSRs
• Conduct case follow-ups with healthcare professionals and partners
• Ensure compliance with regulatory reporting timelines
• Maintain accurate pharmacovigilance documentation and records
• Support signal detection and safety review activities
• Assist with audits, inspections, and internal quality checks
• Collaborate with internal teams and external partners
• Support maintenance of the Pharmacovigilance System Master File PSMF
• Escalate safety concerns according to internal procedures