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.

As a Senior CRA, you will monitor clinical trial sites, ensure compliance with regulations, manage site performance, and train staff to maintain trial standards.

The Senior CRA will oversee clinical trial activities, ensuring adherence to protocols and regulatory requirements while managing multiple sites and projects.

Lead investigator engagement and site-level strategy across clinical trials, driving enrollment, quality, inspection readiness, and cross-functional collaboration. Build long-term investigator relationships, influence protocol feasibility and recruitment, manage vendor oversight, and support post-marketing safety studies where applicable. Requires oncology expertise and frequent travel.

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 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.

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.

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

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.

The Clinical Site Associate supports clinical trial operations, manages site communications, maintains documentation, and ensures compliance for site readiness.

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.

Support clinical study teams across start-up to close-out: maintain TMF and study systems, manage shared team spaces, track study information and budgets, produce study-level reporting, support audit/inspection readiness, quality control documentation, coordinate investigator meetings, translations, and Independent Oversight Committee activities while ensuring GCP and SOP compliance.

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 oversee site compliance, conduct visits, monitor patient safety, and collaborate with cross-functional teams in clinical studies.