Principal Analyst, Statistical Programming
Neurocrine Biosciences
September 04, 2026
Full-time
On-site
San Diego, CA
Clinical Research and Development
Role: Lead SAS statistical programming within Neurocrine Biosciences' Biometrics function, overseeing programming standards, vendor activities, and project execution for clinical and non-clinical data analysis. Responsibilities: direct and mentor programming teams, develop and validate programming procedures, support regulatory submissions (e.g., CSRs, IB updates), and serve as the primary contact for large, multidisciplinary projects. Requirements: BS/BA in a related field with 6+ years of industry experience and 3+ years in a supervisory role, or advanced degrees with fewer years, with expertise in SAS (Base, Stat, Macro, Graph), CDISC (SDTM, ADaM), and industry standards (ICH, FDA). Preferred skills include project management, leadership, and experience with complex data systems and regulatory documents. HighValue: clinical trial data analysis, SAS programming, CDISC standards, regulatory submission support, leadership in a biometrics setting. WorkSetup: on-site in San Diego; position is not remote.