Processing of Individual Case Safety Reports from all sources in compliance with regulations and
Data entry, quality review and submissions workflow steps
Reconciliation activities for all types of received reports
Work under supervision and mentoring of a more experienced colleague

🎯 Requirements

Life science / bioscience background with pharmacovigilance case processing experience
Experience in Data Entry or QC
End-to-end case processing experience (2-3 years)
ARGUS/LSMV/ArisG experience
Time/issue management, multitasking with attention to detail
Strong interpersonal and communication skills

🎁 Benefits

Training and career development opportunities
Focus on personal and professional growth
Friendly, supportive environment
Global colleagues, English as company language

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