Managing and supporting statistical programming deliverables for multiple clinical studies, the full-time Senior Principal Statistical Programmer will serve as a technical lead and project manager, collaborating cross-functionally to ensure high-quality programming outputs for regulatory submissions and clinical communications in a remote environment. Key responsibilities: Lead and manage multiple studies, overseeing all aspects of statistical and clinical programming deliverables Represent the Statistical Programming team in meetings to address project deliverables and timelines Write, test, and validate SAS programs for analysis datasets, tables, listings, and graphs for regulatory submissions Required qualifications: Master's degree in Computer Science, Statistics, Mathematics, Life Sciences, or a related field, or equivalent experience Minimum of 5 years of clinical research programming experience using SAS Expert-level knowledge of CDISC methodologies and experience with SDTM and ADaM standards Experience leading centralized Statistical Programming teams, particularly in oncology trials Familiarity with FDA, EMEA, and CFDA clinical trial and regulatory submissions