Jobs 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.

The Feasibility Principal Analyst leads feasibility activities for clinical studies, analyzes data for enrollment strategies, and mentors junior team members.

As a Clinical Research Associate, you will conduct site visits, ensure data integrity and patient safety, and collaborate on study documentation.

Oversee and monitor clinical trial sites to ensure GCP and protocol compliance, conduct site visits, resolve issues, ensure data integrity, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships to support trial execution.

As a Global Study Manager, you will oversee clinical budgets, develop monitoring plans, manage study start-ups, drive enrollment, and foster relationships with stakeholders.

As Global Study Lead, you will manage clinical trial aspects, focusing on budget oversight, study monitoring, enrollment, and stakeholder relations.

As a Global Study Manager, you will lead projects, manage cross-functional teams, and ensure successful project execution while mentoring team members.