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.
Responsible for supporting Evidence, Value, and Access (EVA) Project Management activities, including resource review and allocation, coordination of meetings, and management of documents. Provide administrative support and collaborate on internal projects and process improvements.
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.