Senior Statistical Programmer leading statistical analyses/reports with R programming at ICON, a global healthcare intelligence and clinical research organization.
IP
ICON plc
Currently Hiring
About the company
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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53 jobs found
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 managing and analyzing laboratory data for clinical research at ICON. Ensuring data accuracy, integrity, and compliance with regulatory standards in a diverse team.
Clinical Supplies Project Manager providing scientific, technical, and regulatory support in pharmaceutical development at ICON. Overseeing supply management and project teams in a collaborative environment.
Analyst role in clinical research systems and reporting at ICON, fostering a culture of innovation. Engaging with users for support and improving system processes.
Senior Statistical Programmer at ICON developing SAS programs for clinical trial data analysis. Collaborates with biostatisticians, ensuring compliance with regulatory standards in a dynamic team environment.
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.