Teams at ICON plc

Perform site qualification, initiation, monitoring, and close-out visits for clinical trials, ensuring 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.

The Study Start Up CRA is responsible for site selection, start up activities, ensuring compliance with relevant regulations, and collaborating with various stakeholders to meet study timelines.

As a Clinical Research Associate, you will conduct site visits, ensure data integrity and patient safety, and collaborate on study documentation.