Pharmacovigilance Associate

📋 Description

• Providing support to other activities undertaken by the project team on behalf of the client and
• Performing activities in the scope of ICSR management unit within agreed extent and timeframe
• 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)

🎯 Requirements

• Life science graduate (pharmacy, nursing, other healthcare related qualification) or experience in
• 0-1 year of experience in pharmacovigilance (desirable but not required)
• Organization skills including attention to detail
• Management skills including time and issue management
• Advanced English (spoken, written)
• Advanced MS-Office literacy

🎁 Benefits

• Training and career development opportunities internally
• Strong emphasis on personal and professional growth
• Friendly, supportive working environment
• Opportunity to work with colleagues worldwide (English company language)