Jobs 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.

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.

Oversee day-to-day clinical laboratory operations supporting clinical trials: supervise staff, ensure accurate and timely sample processing, maintain regulatory compliance and data integrity, streamline workflows, provide training and mentorship, and coordinate with cross-functional teams and external stakeholders to resolve sample-related issues.

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.