Jobs at ICON plc

Coordinate and perform clinical trial monitoring activities, maintain study documentation, handle sponsor queries, support study setup and feasibility, ensure protocol and regulatory compliance, and build relationships with investigators and site staff. Travel (~60%) required.

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.

Lead and conduct clinical trial monitoring for oncology studies, ensuring GCP and protocol compliance. Manage multiple sites, perform site visits, resolve issues, support data integrity and reporting, train site staff and mentor other CRAs, and collaborate with cross-functional teams to maintain trial quality.

Lead onsite and remote monitoring for oncology clinical trials, ensuring data integrity, subject safety, TMF reconciliation, regulatory readiness, site activation, training, KRI monitoring, CAPA implementation, and site relationship management.

Lead site-facing clinical monitoring for oncology studies: conduct selection, initiation, routine monitoring, and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor safety and drug accountability; support recruitment/retention; resolve data queries; escalate risks and coordinate with cross-functional clinical teams.

Support clinical study operations: prepare reports and meeting materials, manage TMF/CTMS/SharePoint, assist document reviews (ICF/CRFs), track site activation/enrolment and monitoring, support registry postings and vendor oversight, and help with study close-out activities and SOP initiatives.

Serve as primary sponsor-site contact for oncology (myelofibrosis) trials, perform site selection/initiation/monitoring/close-out visits, ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor safety reporting (AE/SAE/PQC), support recruitment/retention, oversee drug accountability, resolve data queries, track site budgets/payments, and escalate risks while collaborating 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%.

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, 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.

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.

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.