Job Description
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
Study Review Specialist I
Location: Mexico (Office Based in Mexico City only)
As a Study Review Specialist I you will be responsible for reviewing and approve global Critical Package Documents (CDPs) prior to IP release in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable country regulations/guidelines and the principles of ICH/GCP, ensuring the highest quality and accuracy of documentation.
What You Will Be Doing:
Perform timely and accurate task progress communication and data entry of all relevant CDP Review and Approval activities into the appropriate tracking system.
Ensure CDP ...
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