Jobs at ICON plc

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.

Lead and coordinate oncology clinical trials including start-up, recruitment, protocol execution, training, monitoring, adverse event reporting, sponsor relations, internal quality review, and cross-site travel within the Accellacare network.

Lead and perform clinical trial monitoring and site management for oncology Phase II/III studies, ensuring ICH GCP and local regulatory compliance, site start-up, source data verification, SAE reporting, IP accountability, issue escalation, and documentation. Acts with limited oversight and may lead complex studies or serve as a subject-matter expert.

Provide day-to-day administrative and coordination support for clinical research sites: scheduling visits, maintaining participant records and CTMS data, processing payments and invoices, answering reception calls, supporting lab and supply tasks, assisting CRCs with documentation and study closeouts, and traveling between local network sites.

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

Conduct and manage 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 prepare study documentation and reports. Role requires extensive travel and independent monitoring experience.

Serve as primary site contact for sponsor, perform site selection/initiation/routine/close-out visits, ensure ICH-GCP and regulatory compliance, maintain CTMS and eTMF documentation, monitor safety reporting (AE/SAE/PQC), support recruitment/retention, oversee drug accountability, resolve data queries, escalate risks, and collaborate with cross-functional clinical teams.

Manage site identification, qualification, and activation for cross-therapeutic clinical trials with a start-up focus. Conduct SQVs, coordinate regulatory and contract documents, drive site onboarding to Green Light, monitor KPIs and timelines, support inspections, and act as primary contact between sites, study teams, and stakeholders.

The Clinical Research Associate will monitor sites for compliance, manage documentation, ensure patient safety, facilitate training, and oversee drug accountability in oncology trials.

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.

Manage and monitor Oncology Phase I clinical trial sites, conducting remote and on-site visits, ensuring data integrity, subject safety, inspection readiness, TMF reconciliation, KRI review, CAPA implementation, site activation and training, and supporting regulatory inspections.

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.

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%).

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.

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.

Manage investigator engagement and site strategy to drive enrollment, ensure data quality and inspection readiness, and provide scientific leadership. Build strategic site relationships, influence protocol feasibility, collaborate cross-functionally, oversee vendor monitoring, and support post-marketing safety studies where applicable.