Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to be fully embedded with one general pharmaceutical client. You will implement reporting and analysis activities for sponsor clinical trials, ensuring data quality and regulatory compliance.As a principal programmer you will lead SDTM/ADaM workstreams, supervise CROs, and contribute to study reports and regulatory submissions in a remote, sponsor-dedicated environment.#J-18808-Ljbffr