Collect, assess, and process adverse event reports
Manage safety inbox and acknowledge case receipt
As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information
Job Summary
As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information.
Your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance.
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
Matching Summary
As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information.
Skills & Requirements
Must-have
Post-Marketing Surveillance case processing
collect, assess, and process adverse event reports
Manage safety inbox and acknowledge case receipt
Enter case details accurately and write narratives
Code events, drugs, and medical history using MedDRA/WHO-DD
Apply correct product labeling and perform QC checks
Finalize case processing and generate queries
Process literature ICSRs and maintain compliance
Nice-to-have
cross-functional team collaboration
maintain current knowledge of regulations
mentor new joiners and review SOPs
high standards of quality and compliance
Key Requirements
Minimum 2 years of experience in safety background