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.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
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 case processing
adverse event reporting
regulatory requirements
MedDRA/WHO-DD coding
literature ICSRs
Nice-to-have
collaboration with stakeholders
high standards of quality
patient safety focus
inclusive environment
Key Requirements
Minimum 2 years of experience in safety background
Direct involvement in case processing
Solid experience in Post Marketing Surveillance case processing