Pharmacovigilance Assistant II

About the role

As a Pharmacovigilance Assistant II at ICON, you will ensure the accurate collection, processing, and reporting of safety data for clinical trials and marketed products.

What you'll do

• Take responsibility for pharmacovigilance and drug safety deliverables, applying your skills to ensure quality and efficiency
• Overseeing the collection, processing, and timely reporting of adverse event reports in compliance with regulatory requirements
• Ensuring accurate data entry and maintenance of pharmacovigilance databases, reviewing reports for consistency and completeness
• Assisting in the preparation of periodic safety reports, including risk-benefit analyses, for regulatory submissions and sponsors
• Collaborating with internal teams and external stakeholders to resolve queries related to safety data and pharmacovigilance activities

What you need

• Pharmacovigilance
• Regulatory affairs
• Documentation
• Communication
• Clinical research
• B.Sc

Good to have

• Two-wheeler