Teams at ICON plc

Perform site qualification, initiation, monitoring, and close-out visits for obesity and cardiology clinical trials. Ensure protocol compliance, data integrity, patient safety, resolve data queries, and support study documentation and clinical study report preparation while collaborating with investigators and site staff.

The Study Start Up CRA is responsible for site selection, start up activities, ensuring compliance with relevant regulations, and collaborating with various stakeholders to meet study timelines.

Lead site management and monitoring for Oncology clinical trials, performing on-site and remote visits, ensuring data integrity and subject safety, managing TMF/essential documents, driving site activation and engagement, monitoring KRIs, implementing CAPAs, supporting IRB/EC submissions and regulatory inspections, and mentoring/joining oversight activities.