Processing ICSR reports from all sources per regulations and client timelines
Performing ICSR follow up and SAE/SUSAR management tasks
Reconciliation with clinical partners and data quality checks
Maintaining data protection and product quality complaint handling
Medical Information interaction and MedDRA/WHO coding
Generating database outputs and monthly client reports; managing workflow and resources

🎯 Requirements

Life science graduate, pharmacy, nursing or related experience in pharmacovigilance
Minimum 1 year PV work experience
Strong organizational, time and issue management skills
English advanced (spoken, written)
Advanced literacy with MS Office

🎁 Benefits

Global pharmacovigilance environment across Europe, North America, Asia, and Australia
Culture of kindness, flexibility, growth and belonging
Opportunities to grow while protecting patients

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