Jobs at ICON plc

Monitor and manage clinical trial site activities including qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, patient safety, query resolution, and contribute to study documentation and reporting. Collaborate with investigators and site staff to support high-quality trial conduct.

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.

Conduct site qualification, initiation, monitoring, and close-out visits for oncology clinical trials. Ensure protocol compliance, data integrity, patient safety, resolve queries, and contribute to study documentation and reports.

Oversee cardiovascular clinical trials, ensuring compliance with regulations while managing site relationships and communication. Requires 3 years of monitoring experience and strong problem-solving skills.

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

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.

The Senior Clinical Research Associate manages monitoring for cardiovascular clinical trials, ensuring compliance with FDA regulations and guiding teams to resolve site issues effectively.

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

Manage and monitor oncology clinical trials ensuring compliance with ICH GCP and local regulations. Perform site qualification, startup, monitoring (on-site/remote), source data verification, SAE reporting, IP accountability, document reconciliation, and trial tracking. Provide leadership, act as subject matter expert, escalate and resolve site issues, and support feasibility, site selection, and contract/budget activities.

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.

Monitor early-stage (Phase I) clinical trials: conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; resolve data queries; collaborate with investigators and prepare/review study documentation including protocols and clinical study reports.

Lead on-site clinical monitoring for oncology (myelofibrosis) trials: conduct site selection, initiation, routine and close-out visits; ensure ICH-GCP and SOP compliance; maintain CTMS/eTMF documentation; monitor safety (AE/SAE/PQC) and drug accountability; support recruitment/retention; resolve data queries; track site budgets/payments; escalate risks and collaborate with cross-functional clinical teams.

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.

Senior Site Monitor responsible for planning and conducting on-site and remote monitoring across Phase I-IV studies. Ensures site compliance with protocol, data quality, and participant safety, conducts source data verification, manages site communications, supports RBQM processes, and participates in audits and inspections.

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

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.

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.