Mexico or Brazil. Remote.

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.

What You Will Do:

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

• Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics.
• Collaborating with cross‑functional teams to facilitate communication and address site‑related issues effectively.
• Maintaining accurate records of site activities and contributing to the preparation of mon...