EPM is looking for Senior Statistical Programmer to join a highly respected full ‑ service CRO with deep roots in statistical excellence, this organization supports global pharma, biotech, and medical device innovators with high ‑ quality clinical research solutions. This organization takes a truly holistic approach to clinical research, valuing not only scientific excellence but also the well ‑ being of the people behind the work. It fosters a supportive, positive environment where collaboration, balance, and respect are central to everyday operations. Design and define study data tabulation structures and analysis datasets for clinical trials, including integrated datasets (ISS/ISE), ensuring alignment with industry standards, statistical needs, and sponsor requirements. Build high ‑ quality analysis datasets based on approved specifications and independently validate datasets created by other programmers or statisticians. Program SAS code to produce accurate tables, listings, figures, and statistical outputs, as well as to independently validate outputs produced by others. Develop and test SAS code for database checks, data listings, and ongoing data review activities. Maintain thorough documentation of programming work and archive datasets and code according to company SOPs. Expand expertise in additional programming areas as needed and provide technical support to junior Statistical Programmers. Contribute to improving programming processes and help define therapeutic area or client ‑ specific programming standards when acting as a lead programmer. Requirements: Master ' s degree in Math/Statistics (or related field) 5 years of experience in statistical programming within clinical trials