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

Experience in Pharmacovigilance case processing
Life science / bio medical background – healthcare related degree (chemistry, biology
Excellent communication (written and verbal) skills
Organization skills, including attention to details and multitasking
Delegation skills
Planning and time management

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