As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials, while ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct.
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Join our dynamic team as a Clinical Research Associate at ICON, and play a pivotal role in advancing innovative treatments. Responsibilities include conducting site visits, ensuring protocol compliance, performing data review, and contributing to study documentation.
Join the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence, as a CRA homebased in France. You will have ownership of investigator sites for assigned studies and be responsible for the successful management of the site right through to close-out. You will also plan and conduct various site visits, develop effective relationships with investigator site staff, and ensure integrity of clinical data.