Sr. Principal Analyst, Statistical Programming

Role: Lead statistical programming for neurobiopharmaceutical clinical programs, overseeing data analysis, programming standards, and vendor management. Responsibilities: provide technical leadership across biometrics, develop programming infrastructure, mentor teams, manage vendor selection, and support regulatory submission documentation such as SDTM, ADaM, and define.xml files. Requirements: BS/BA in computer science, statistics, or related field with 8+ years industry experience and 2+ years in a supervisory role; or Master’s degree with 6+ years; or PhD with 4+ years. Expertise in SAS (Base, Stat, Macro, Graph), CDISC data standards, and FDA/ICH guidelines is essential. Preferred skills include experience with SDTM/ADaM datasets, cross-functional project management, and regulatory submissions. High-Value: Biopharma, clinical development, statistical programming leadership, regulated environment, emphasis on data standards, with a focus on neuroscience or neurological disorders. WorkSetup: Not specified.