Teams at ICON plc

Perform site selection visits, manage initial Health Authority and IRB submissions, negotiate site budgets, and prepare for site initiation visits (study access, lab kits, investigational product logistics). Partner with a global pharmaceutical client on multicenter studies while maintaining limited travel.

Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensure protocol compliance, data integrity, and patient safety. Collaborate with investigators and site staff, review data and resolve queries, and contribute to study documentation including protocols and clinical study reports.

As a Clinical Research Associate, you will coordinate clinical trials, ensure regulatory compliance, and maintain study documentation, while establishing relationships with stakeholders.