Senior Clinical Trial Manager ensuring successful clinical study delivery and effective management of clinical budgets at ICON. Overseeing study integrity and fostering relationships with stakeholders.
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life.
We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.
We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries.
We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
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Senior Clinical Trial Manager ensuring successful clinical study delivery and effective management of clinical budgets at ICON. Overseeing study integrity and fostering relationships with stakeholders.
Lab Data Analyst I at ICON plc managing and analyzing laboratory data for clinical research studies. Ensuring data accuracy, integrity, and compliance with regulatory standards.
Lead KCR Emerging Oncology Biotech global operations for ICON plc. Direct project management, clinical monitoring, regulatory, contracts, vendor management, and strategic growth.
Senior Clinical Trial Manager at ICON leading clinical operations and study delivery in China. Responsible for project leadership, risk mitigation, client relationships, and cross‑functional project management.
Statistical Programmer II at ICON developing validated SAS/R/Python programs for clinical trial analysis and reporting. Collaborates with biostatisticians, ensures regulatory compliance, mentors junior programmers.
Senior Data Scientist developing data models, ML algorithms and BI reports for clinical trials at ICON plc. Coordinate stakeholders and ensure model performance and data accuracy.
Manage 10 - 15 clinical lab studies, act as sponsor contact and represent ICON at meetings. Ensure GCP compliance, reporting, and ICOLAB support to sponsor personnel.
Senior Project Manager overseeing ICON Central Laboratories study setup and client management. Ensuring compliance with Good Clinical Practice and mentoring junior PMs.
Principal Biostatistician managing clinical trials and statistical analyses for ICON plc. Lead biostatistical efforts in drug development across multiple sponsors focusing on Vaccines, Oncology, and Rare Diseases.
Project Manager II overseeing clinical laboratory services and client satisfaction in clinical trials at ICON plc. Managing projects, ensuring compliance, and facilitating communication with sponsors and internal teams.
Statistical Programmer II role at ICON focusing on statistical program development and execution for clinical trial analysis. Collaborating with diverse teams to ensure data integrity and compliance.
Medical Director responsible for strategic medical leadership and guidance on project teams at ICON plc. Collaborating on compliance and providing expert consultation in oncology projects.