Senior Pharmacovigilance Associate

Responsibilities

• Process Individual Case Safety Reports (ICSRs) from all sources in compliance with regulations and client requirements
• Perform ICSR follow-up and SAE/SUSAR management including unblinding and clinical trial reconciliation
• Handle MedDRA and WHO coding
• Manage Product Quality Complaints and interact with Quality Assurance
• Support PV processes and act as Local Contact Person for Pharmacovigilance (LCPPV) as needed
• Manage database outputs and reports for monthly client reporting

Requirements

• Life science degree, pharmacy, nursing, or related healthcare qualification
• Minimum 1 year of experience in pharmacovigilance
• Advanced English proficiency (spoken and written)
• Strong organizational skills and attention to detail
• Proficiency in MS Office

About the Company

PrimeVigilance is a global pharmacovigilance specialist helping clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marketing surveillance.