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.

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

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 site management and monitoring for oncology clinical trials, ensuring data integrity, subject safety, inspection readiness, and regulatory compliance. Perform on-site and remote monitoring, train and mentor CRAs, manage TMF/essential documents, drive site activation and engagement, and implement CAPA and KRI oversight.

Lead on-site clinical monitoring for oncology/hematology trials: conduct site selection, initiation, routine and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor patient safety and AE/SAE reporting; oversee drug accountability, support recruitment and retention, resolve data queries, track site budgets, and escalate risks to clinical teams while collaborating cross-functionally.

Serve as primary contact between investigational sites and sponsor to conduct site selection, initiation, routine monitoring, and close-out. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety (AE/SAE/PQC), support recruitment and drug accountability, resolve data queries, track site training and budgets, escalate risks, and collaborate with cross-functional clinical teams.

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.

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

Lead and perform monitoring of Phase I oncology clinical trial sites to ensure GCP, protocol and regulatory compliance. Conduct site visits, resolve issues, provide training and guidance to site staff and CRAs, collaborate with cross-functional teams, maintain data integrity, and build stakeholder relationships. 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%).

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 and perform clinical trial monitoring to ensure protocol, regulatory, and GCP compliance. Conduct site visits, resolve issues, support data integrity, train and mentor site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships to drive successful trial execution. Travel approximately 60%.

Lead and perform clinical trial monitoring to ensure protocol adherence, GCP and regulatory compliance. Conduct site visits, resolve issues, support data integrity, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships to drive high-quality trial execution.

Serve as primary contact between sites and sponsor for oncology (myelofibrosis) trials. Perform site selection, initiation, routine monitoring, and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor safety reporting (AE/SAE); support recruitment, drug accountability, data query resolution, and cross-functional escalation.

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.