Processing of Individual Case Safety Reports from all sources in compliance with regulations and
Independent SAE/SUSAR management (submissions, unblinding, clinical trial reconciliations).
Prepare database outputs for periodic reporting (PBRER, DSUR, PADER).
Mentor and train junior staff, optimize and develop procedures.

🎯 Requirements

Life science / biomedical background with healthcare-related degree.
Demonstrated case processing experience with attention to detail.
Time and issue management, organization, multitasking.
Strong interpersonal and communication skills.
Advanced English (verbal and written) at least C1.

🎁 Benefits

Global pharmacovigilance environment with patient safety focus.
Collaborative, flexible culture with opportunities for growth.

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