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As a Clinical Research Associate II, you will conduct trials, ensure compliance, analyze data, and prepare study documentation in a collaborative environment.

The Senior PK Scientist will author clinical pharmacology protocols, perform PK/PD analyses, develop analysis plans, and ensure compliance in clinical trials.

The Director of Tax will oversee tax strategies, manage risks, ensure compliance across countries, and lead a team of tax professionals while maintaining relationships with stakeholders.

Lead the biostatistics consulting practice by providing statistical guidance, overseeing clinical trial design, and managing cross-functional teams for regulatory compliance and innovative solutions.

The Business Intelligence Developer will design, develop, and implement BI solutions; collaborate with stakeholders; maintain ETL processes; and create dashboards for insights in healthcare.

The PK Scientist will support protocol development, perform pharmacokinetic analyses, and collaborate on clinical pharmacology reporting in clinical trials.

Oversee the planning, execution, and completion of clinical trials, ensuring compliance with timelines, budgets, and regulations while collaborating with teams and managing site relationships.

Lead the creation and validation of SAS programs for statistical analysis, ensuring data integrity and collaboration with biostatisticians. Mentor junior programmers and contribute to regulatory submissions.

The Senior Director of Finance will oversee accounting and reporting, ensure compliance with US GAAP and IFRS, and guide financial strategy at ICON plc. Responsibilities include leading financial audits, managing complex accounting issues, and collaborating with other finance teams on strategic initiatives.

The Central Monitor oversees clinical trials, ensuring data quality, implementing monitoring strategies, identifying risks, and improving trial efficiency through data-driven insights.