Jobs at ICON plc

Serve as primary contact between sites and sponsor for oncology (myelofibrosis) trials. Perform site selection, initiation, routine monitoring, and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor safety reporting (AE/SAE); support recruitment, drug accountability, data query resolution, and cross-functional escalation.

Lead on-site clinical monitoring for oncology/hematology trials: conduct site selection, initiation, routine and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor patient safety and AE/SAE reporting; oversee drug accountability, support recruitment and retention, resolve data queries, track site budgets, and escalate risks to clinical teams while collaborating cross-functionally.

Serve as primary contact between investigational sites and sponsor to conduct site selection, initiation, routine monitoring, and close-out. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety (AE/SAE/PQC), support recruitment and drug accountability, resolve data queries, track site training and budgets, escalate risks, and collaborate with cross-functional clinical teams.

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; contribute to study documentation and clinical study reports.

Lead clinical trial monitoring activities to ensure protocol and regulatory compliance, conduct site visits, resolve issues, support data integrity, train site staff and CRAs, collaborate cross-functionally, and maintain strong site relationships to drive successful trial execution.

The Clinical Research Associate will manage clinical trials, ensure compliance and data integrity, and collaborate with site staff and investigators.

Lead end-to-end site selection for assigned clinical studies: develop protocol-specific criteria and recruitment strategies, conduct feasibility and risk assessments, oversee site outreach and team performance, track budgets and timelines, ensure regulatory compliance and data quality, and present recommendations to sponsors. Travel ~15%.

Conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance, data integrity, and patient safety. Review and resolve data queries, collaborate with investigators and site staff, and contribute to study documentation including protocols and clinical study reports. Role requires frequent travel and independent monitoring experience.

Lead cross-functional study teams to plan, execute, and close regional/global clinical trials. Manage scope, timelines, risk mitigation, budgets, enrollment strategy, vendor/TPO oversight, Trial Master File readiness, training coordination, and stakeholder communication to deliver quality trials on time and within budget.

The Clinical Systems Specialist will design and analyze clinical trials, interpret medical data, and support UAT processes within clinical systems.

Monitor clinical trials by conducting site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; review and resolve data queries; and contribute to study documentation and clinical study reports.

Lead 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, perform data review and queries resolution, and contribute to study documentation and clinical study reports.

Monitor and manage clinical trial sites including qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; perform data review and query resolution; collaborate with investigators and site staff; contribute to study documentation and clinical study reports.

Oversee and monitor clinical trial sites to ensure protocol, regulatory and GCP compliance; conduct site visits; manage multiple sites; ensure data integrity and participant safety; train and support site staff; collaborate with cross-functional teams and maintain stakeholder relationships.

As a Clinical Research Associate, you will monitor clinical trials, ensuring adherence to protocols and regulations, conduct site visits, and train staff.

The Clinical Research Associate will conduct monitoring visits, ensure protocol compliance, collaborate with site staff, and maintain data integrity.

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

Oversee and approve scientific and clinical content for assigned medical communications projects; review and fact-check deliverables; mentor and onboard junior writers; produce manuscripts, posters, abstracts, and slide decks; collaborate with account and scientific managers to meet timelines and budgets; support business development with background research and proposal writing; liaise with cross-functional teams including graphics and editorial.

Lead strategy and execution for Oncology Elite site network and relationships. Identify and engage partner sites pre-award, support bid scenarios, monitor post-award delivery, collaborate with clinical operations and project teams, present strategy to clients, and track KPIs to drive process improvements for timely trial start-up and execution.