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Oversee and manage clinical trials, ensuring compliance with timelines, budgets, and regulations while collaborating with cross-functional teams and stakeholders.

The Talent Acquisition Business Partner will execute recruitment strategies, manage the hiring process, analyze metrics, and build relationships to enhance talent acquisition.

The Clinical Research Associate will conduct clinical trial visits, ensure protocol compliance, collaborate with site staff, and maintain data quality.

The Administrative Assistant will manage administrative tasks such as file management, calendar coordination, meeting arrangements, and report compilation to support departmental functions at ICON.

The Global Clinical Project Manager leads and oversees early phase clinical studies in haematology, ensuring timely, budget-compliant delivery while fostering collaboration among cross-functional teams.

As a Statistical Programmer, you will analyze clinical trial data, ensure compliance with regulatory standards, and develop SAS programs for statistical analysis and reporting.

Manage all aspects of clinical trials, ensuring compliance with timelines and regulations, while collaborating with teams and stakeholders.

The Senior Statistical Programmer will develop and validate SAS programs, collaborate with biostatisticians, perform quality control, and enhance programming processes for clinical trials.

Assist in coordinating and administering clinical trials, maintaining documentation, preparing study materials, and tracking trial metrics.

The Investigator Payments Coordinator manages payments to clinical trial investigators, ensures accuracy in financial transactions, and collaborates with teams to support clinical trials.