Principal Statistical Programmer

The Principal Statistical Programmer serves as a senior technical expert responsible for independently developing, validating, and delivering high-quality SAS programming deliverables for clinical trial analysis and reporting. This role ensures the accuracy, quality, and regulatory compliance of study data packages by applying CDISC standards and supporting submission-readiness. The position involves providing technical leadership, collaborating cross-functionally with biostatistics and data management teams, and contributing to the continuous improvement of programming standards and processes.