Senior Pharmacovigilance Associate

📋 Description

• Perform ICSR management activities within timeline and scope
• Process IC SRs from all sources per regulations and client requirements
• Perform ICSR follow up and SAE/SUSAR management activities
• Reconcile clinical data with partners and maintain data protection
• Handle product quality complaints and liaise with QA
• MedDRA and WHO coding; generate database outputs/reports for clients

🎯 Requirements

• Life science graduate, pharmacy, nursing or related pharmacovigilance experience
• Minimum 1 year PV experience; strong organization and multitasking
• Time management and issue tracking skills
• Advanced English (spoken, written) and MS Office

🎁 Benefits

• Global pharmacovigilance team with patient safety focus
• Collaborative, values-driven culture across regions