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)
Personal data protection

Qualifications

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)

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