Senior Clinical Data Programmer — Drive Trial Data Quality

Cytel is seeking an experienced Clinical Programmer in Richmond, Virginia, to write and maintain code for clinical trial data processes. The role requires 4-6 years of experience in clinical programming, proficiency in languages such as SAS and R, and strong knowledge of data structures and regulatory requirements. You will collaborate closely with data managers and statisticians, ensuring compliance with regulatory requirements and continuous improvement of programming practices. This position offers a dynamic team environment where mentorship is encouraged.
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