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.

Monitor clinical trial sites, ensure adherence to protocols, conduct site visits, train staff, and manage relationships for oncology trials.

The Clinical Research Associate acts as the main liaison between investigation sites and sponsors, conducting site visits, ensuring compliance, monitoring patient safety, and managing documentation and site staff training.

Clinical Trial Liaisons provide scientific support to clinical trial sites, optimize patient recruitment strategies, and engage with stakeholders to achieve trial goals. They require strong communication skills and a doctoral degree.

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 and perform site selection, initiation, routine monitoring, and close-out visits. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety and reporting, support recruitment and drug accountability, resolve data queries, track site budgets/payments, and escalate risks while collaborating with cross-functional clinical teams.

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

Lead and manage the Project Management team for imaging projects across clinical research programs. Provide strategic and tactical oversight, ensure process consistency, resource planning, compliance with company policies, stakeholder engagement, and mentor project managers to deliver projects on time, within scope and aligned with corporate strategy and customer expectations.

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.

Support and coordinate clinical trial site monitoring to ensure protocol, regulatory, and GCP compliance; prepare and review regulatory documents; collaborate with cross-functional teams; track site performance and report findings; mentor junior staff and support training initiatives.

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.

As a Senior Clinical Research Associate, you will manage clinical trials, ensuring protocol compliance, data integrity, and patient safety, while collaborating with site staff and preparing study documentation.

As a Clinical Research Associate, you will monitor clinical trials, ensuring adherence to protocols and regulations, conduct site visits, and train staff.

Lead data-driven feasibility and site strategy for clinical studies: assess protocol feasibility, build enrollment projections and scenario models, optimize country/site selection, coordinate global site intelligence, and provide strategic recommendations to improve recruitment timelines and study start-up efficiency.

As a Clinical Research Associate, you will monitor clinical trials, ensuring compliance and data integrity, while collaborating with site staff and investigators.

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.

Lead and manage end-to-end clinical trial site start-up and activation activities. Oversee site identification, feasibility, regulatory submissions, timelines, budgets, and risks. Mentor and lead a study start-up team, collaborate with sponsors and internal stakeholders, and drive process improvements to optimize start-up efficiency and compliance.

The Clinical Research Associate will manage site interactions, ensure compliance, monitor clinical studies, and support data management and recruitment efforts.

Oversee the implementation of IRT solutions for clinical trials, managing project planning, execution, and stakeholder communication.