Jobs at ICON plc

As a Senior Clinical Research Associate, you will manage clinical trials, ensuring compliance with protocols and regulations, mentoring staff, and maintaining site relationships while overseeing multiple projects.

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.

Lead clinical project teams to plan, execute and monitor multi-country clinical trials. Maintain study documents, manage resources, forecast finances, identify and mitigate risks, liaise with clients/vendors, implement CAPAs, and support start-up, metrics reporting, and business development activities.

As a Sr CRA, you will monitor clinical trials, ensure compliance with protocols and regulations, support site staff, and manage relationships with sites and stakeholders.