Pharmacovigilance Specialist

About the role

As a Pharmacovigilance Specialist at ICON, you will be responsible for monitoring the safety of pharmaceutical products by analyzing, interpreting, and reporting adverse event data in accordance with regulatory requirements.

What you'll do

• Take responsibility for pharmacovigilance and drug safety deliverables, applying your skills to ensure quality and efficiency
• Collecting, reviewing, and analyzing adverse event reports to ensure timely and accurate reporting in compliance with regulatory guidelines
• Conducting risk assessments and signal detection activities to identify and evaluate potential safety concerns
• Collaborating with cross-functional teams to support safety-related inquiries and investigations
• Preparing and submitting safety reports and regulatory submissions in a timely manner

What you need

• Pharmacovigilance
• Learning and development
• Regulatory affairs
• Communication
• Any graduate