Cytel is seeking a Senior/Principal Statistical Programmer to work remotely on clinical development programs across therapeutic areas. You will implement reporting and analysis activities, coordinate with CROs, and ensure high-quality, timely outputs for regulatory submissions. The role involves developing SDTM/ADa M specifications, writing SAS and R programs, and supporting CSR preparation under FDA guidelines. This is a sponsor-dedicated position with general client engagement. #J-18808-Ljbffr