Sr. Biostatistician

Role: Serve as the statistical lead for multiple clinical studies within Neurocrine Biosciences' neuroscience portfolio, providing statistical expertise in study design, analysis, and reporting. Responsibilities: develop statistical analysis plans, collaborate on protocol development, review data validation and transfer specifications, monitor CRO performance, support nonclinical and medical teams, and innovate statistical methodologies. Requirements: Master's in statistics or biostatistics with 4+ years of relevant experience or PhD with 2+ years, proficiency in SAS, strong understanding of clinical trial design, regulatory standards (CDISC, FDA), and project management skills. Preferred: direct regulatory authority interaction experience. HighValue: neuroscience therapeutic area, clinical studies across phases, emphasis on data standards and regulatory compliance, supporting drug development from early to late-stage trials. Collaboration includes biometrics, clinical development, medical writing, and external CROs. Work setup: not specified, but typical roles imply office or hybrid environment with emphasis on cross-functional coordination.