Cytel is a global leader in data-science clinical research organizations (CRO), specializing in adaptive trial design and innovative software solutions for drug development. With over four decades of experience, Cytel leverages extensive data insights to enhance success rates and deliver better patient outcomes through a comprehensive suite of services including trial design, statistical programming, and real-world analytics. Headquartered in Cambridge, Massachusetts, the company serves clients across North America, Europe, and Asia.
We are seeking an experienced Clinical Programmer with a strong background in clinical programming to write and maintain code for clinical trial data processes, ensure accurate and timely delivery of clinical trial data, and collaborate with stakeholders to design and implement clinical data flow.
Cytel is a global leader in data-science clinical research organizations (CRO), specializing in adaptive trial design and innovative software solutions for drug development. With over four decades of experience, Cytel leverages extensive data insights to enhance success rates and deliver better patient outcomes through a comprehensive suite of services including trial design, statistical programming, and real-world analytics. Headquartered in Cambridge, Massachusetts, the company serves clients across North America, Europe, and Asia.
ICON plc