Sr. Principal Statistician, Biostatistics

Role: Senior Principal Statistician supporting clinical trial design, analysis, and regulatory submissions across Phase I-IV studies in oncology and neuroscience. Responsibilities: lead statistical aspects of study design, develop analysis plans, validate data, collaborate cross-functionally with clinical development teams, oversee external vendors, and contribute to regulatory interactions and documentation. Qualifications: MS/MPH in statistics or related field with over 4 years of industry experience or PhD in a relevant discipline; expertise in complex statistical methods, sample size calculations, and regulatory standards like ICH Guidelines; proficient in SAS and R; knowledge of Bayesian/adaptive designs preferred. HighValue: involvement in late-stage clinical trials (Phases I-IV), expertise in oncology/neuroscience indications, and familiarity with global regulatory requirements. WorkSetup: not specified, likely hybrid or office-based based on typical biopharma roles.