Jobs at ICON plc

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.

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.

Lead planning, coordination, and delivery of clinical document translations. Manage vendors, stakeholders, budgets, timelines, and quality controls. Implement and evaluate AI-enabled translation tools and oversee SME post-editing to ensure regulatory-compliant, high-quality translations for clinical documents.