Associate Director, Statistical Programming

Role: Serve as Program Lead Statistical Programmer for one or more clinical programs at Neurocrine Biosciences, providing strategic and technical leadership in statistical programming across early to late-phase studies. Responsibilities: develop efficient analysis and reporting approaches, support regulatory submissions, establish programming standards, oversee vendor activities, and mentor junior staff. Collaborate cross-functionally within Biometrics to optimize programming practices and ensure high-quality, scalable deliverables. Requirements: BS/BA in related field with 10+ years or advanced degree with 8+ years biopharma experience; expert-level SAS skills; managerial experience; strong knowledge of clinical data standards (SDTM, ADaM, CDISC); proven leadership in cross-functional teams and vendor oversight. HighValue: extensive experience in biopharmaceutical clinical development, with emphasis on early-phase or proof-of-concept studies, regulatory submission support, and complex data systems. Familiarity with neuropsychiatric, neurological, or endocrine indications is advantageous. WorkSetup: primarily on-site with leadership responsibilities; no specific travel mentioned.