Jobs at ICON plc

Support clinical study operations including eTMF and CTMS setup and maintenance, document control, trial registrations, meeting coordination, finance and vendor tracking, monitoring oversight, clinical supplies coordination, QC of TMF, and support during audits and inspections per ICH/GCP and sponsor SOPs.

Support clinical study operations including eTMF and CTMS setup and maintenance, document control, sponsor and regulatory compliance (ICH/GCP), trial registration, finance tracking, monitoring visit oversight, supplies coordination, meeting coordination and minute-taking, logs and trackers maintenance, and audit/inspection support.

The Senior Clinical Research Associate will manage site activities and ensure compliance during Oncology clinical trials, focusing on data integrity and subject safety.

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

Leads clinical data risk management and central monitoring for multiple clinical studies. Responsibilities include evaluating trial data for risks and trends, selecting KRIs, overseeing signal tracking and quality control, analyzing discrepancies, developing mitigation strategies, supporting data governance and compliance, coordinating stakeholders, and mentoring junior staff.

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.

Conduct clinical trial site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; review data and resolve queries; and contribute to study documentation, protocols, and clinical study reports. The role requires at least two years of CRA experience, relevant scientific or healthcare education, strong organizational and communication skills, and approximately 60% travel.

Oversee and monitor clinical trial sites to ensure protocol, regulatory, and Good Clinical Practice compliance. Conduct site visits, resolve issues, support trial execution, and collaborate with cross-functional teams on data collection and reporting. Train and guide site staff and other CRAs, maintain stakeholder relationships, and manage multiple sites and projects while driving data integrity and continuous improvement. The role requires approximately 60% travel.

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

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%.

Manage planning, execution, and delivery of IRT solutions for clinical trials. Define scope, timelines, budgets, and oversee UAT, vendor relationships, and cross-functional stakeholder communication. Ensure regulatory compliance, drive project efficiency, and stay current on IRT industry trends.

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.

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.

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.

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; perform data review and query resolution; and contribute to study documentation including protocols and clinical study reports.

Monitor clinical trials (site qualification, initiation, monitoring, close-out), ensure protocol compliance, data integrity, and patient safety. Review and resolve data queries, collaborate with investigators and site staff, and contribute to study documentation and clinical study reports. Approximately 60% travel; requires CRA monitoring experience and ICH-GCP knowledge.

Conduct and coordinate clinical trial monitoring activities, maintain study documentation, manage sponsor queries, support study setup and feasibility, ensure regulatory and protocol compliance, and build collaborative relationships with investigators and site staff. Role requires frequent travel (~60%).

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.

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