Senior Pharmacovigilance Associate

📋 Description

• Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable
• Performing ICSR follow up
• SAE/SUSAR Management (unblinding, clinical trial reconciliation, protocol review, Safety Management
• Reconciliation (clinical, partners)
• Personal data protection
• Product Quality Complaint handling and interaction with Quality Assurance

🎯 Requirements

• Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in
• Minimum 1 year of work experience in pharmacovigilance
• Organization skills, including attention to detail and multitasking
• Management skills, including time and issue management
• English - advanced (spoken, written)
• Advanced literacy (MS Office)