Providing support to project team activities on behalf of client and company
Processing Individual Case Safety Reports (ICSRs) in compliance with regulations and client
Performing ICSR follow-up
SAE/SUSAR Management including unblinding, clinical trial reconciliation, protocol review, Safety
Reconciliation (clinical, partners)
Personal data protection

🎯 Requirements

Life science/biomedical background (chemistry, biology, biotechnology, veterinary science)
Demonstrated experience in Pharmacovigilance case processing
Excellent communication skills (written and verbal)
Organization skills, attention to detail, multitasking
Delegation skills
Planning and time management

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