Teams 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.

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.