Senior Pharmacovigilance Reporting Associate

Senior Pharmacovigilance Reporting Associate (Must Have: Safety Submission experience)

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a Senior Pharmacovigilance Reporting Associate at ICON, you will be essential in ensuring accurate and timely reporting of safety data related to pharmaceutical products.

**What You Will Do:**

Your experience in pharmacovigilance and drug safety will be key in delivering high-quality outcomes and mentoring colleagues.

Key responsibilities include:

+ Preparing and submitting adverse event reports and safety data in accordance with regulatory requirements and internal policies, ensuring accuracy and completeness.
+ Collaborating with clinical and regulatory teams to review and analyze saf...

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Submit your application today and join our talented team at ICON Clinical Research.

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