Senior Pharmacovigilance Associate

📋 Description Process ICSR from all sources per regulations and timelines Perform ICSR follow up and SAE/SUSAR management Reconciliation (clinical, partners) and data protection Medical Information interaction and MedDRA/WHO coding Produce database outputs and reports for monthly client reporting Support PV processes and act as Local Contact Person as needed 🎯 Requirements Life science graduate or healthcare qualification; PV experience Minimum 1 year PV experience Strong organization, time management, and attention to detail English advanced (spoken, written) Advanced MS Office skills 🎁 Benefits Global pharmacovigilance specialist environment Culture of kindness, flexibility, growth and belonging Opportunities for professional development