Full-time

Pharmacovigilance Assistant

Posted by ICON Clinical Research • June 06, 2026

📍 Mexico City, Mexico, Mexico
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Description

Home Based - CDMX

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 Pharmacovigilance Assistant I at ICON, you will support the collection, documentation, and reporting of safety data related to medications and clinical trials.

**What You Will Do:**

You will contribute to pharmacovigilance and drug safety activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

+ Supporting the collection, review, and processing of adverse event reports related to clinical trials and marketed products.
+ Ensuring timely and accurate data entry of safety information into pharmacovigilance databases.
+ Assisting in the preparation and submission of safety reports to regulatory ...

Ready to Seal the Deal?

Submit your application today and take the next step in your career with ICON Clinical Research.

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