Jobs at ICON plc

Lead feasibility informatics strategy for clinical trial proposals and awarded feasibility projects. Provide data-driven feasibility analyses using internal/external data, support bid defenses, manage delivery and handover to site identification, assess risks, and collaborate with cross-functional teams to meet sponsor objectives.

Lead creation, review, and optimisation of global and local informed consent forms (ICFs). Advise study teams on consent strategy, manage translations/version control, liaise with sponsors, ethics committees and regulators, develop templates and guidance, and provide training and mentorship to junior staff while managing multiple complex clinical studies.

Lead and perform clinical trial monitoring for Phase I oncology studies, ensuring GCP and protocol compliance, conducting site visits, mentoring CRAs, collaborating cross-functionally, and driving data integrity and site performance. Travel approximately 60%.

Lead clinical trial monitoring to ensure protocol and regulatory compliance, conduct site visits, resolve issues, mentor CRAs, collaborate with cross-functional teams, and maintain data integrity and site performance. Travel required (~60%).

Monitor and manage clinical trial activities including site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; resolve data queries; collaborate with investigators and site staff; and contribute to study documentation and clinical study reports. Approximately 60% travel required.

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

Lead investigator engagement and site-level strategy for immunology clinical trials: drive enrollment, build long-term investigator relationships, optimize feasibility and protocol conduct, ensure inspection readiness, oversee vendor quality, and collaborate cross-functionally to meet clinical milestones and improve site performance.

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.

Lead investigator engagement and site strategy for clinical trials, driving enrollment, site selection, risk planning, and quality. Build high-trust investigator relationships, influence protocol understanding, collaborate cross-functionally and with vendors, and support inspection readiness and study closeout. Focused oncology experience required.

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 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.

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%.

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.

Lead investigator engagement and site strategy to drive enrollment and data quality for clinical trials. Build strategic relationships with investigators, co-create recruitment plans, monitor site performance, ensure inspection readiness, oversee vendor monitoring, and contribute scientific insights to protocol design and study conduct. Support post-marketing safety studies where applicable and collaborate cross-functionally to remove operational barriers and optimize trial delivery.