Process Individual Case Safety Reports from all sources in compliance with regulations and client
Manage SAE/SUSAR submissions, unblinding, and clinical trial reconciliations
Prepare outputs for periodic safety reports (PBRER, DSUR, PADER, etc.)
Mentor and train junior staff and optimize procedures

🎯 Requirements

Life science / biomedical background with pharmacovigilance case processing experience
Strong time and issue management, organization, multitasking
Excellent interpersonal and communication skills
Advanced English skills, verbal and written (C1)

🎁 Benefits

Global pharmacovigilance environment across regions
Collaborative and supportive team culture
Focus on growth, flexibility, and belonging

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