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.
As a Principal Statistical Programmer, you will work on clinical development programs on different therapeutic areas and oversee CRO programmers to ensure high-quality data summaries. You will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.
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.
Cytel