Director, Biostatistics, Early Phase

Role: Lead statistician for oncology clinical trials at a late-stage biopharma developing RAS-targeted therapies. Objectives: provide statistical leadership for study design, analysis, and reporting; collaborate across functions; support regulatory submissions and publications. Responsibilities: serve on study teams, develop statistical analysis plans, ensure data quality, and contribute to SOPs; keep current on statistical advances relevant to oncology and biopharma. Requirements: Ph.D. or M.S. in Statistics/Biostatistics; 8+ years (Ph.D.) or 12+ years (M.S.) industry experience; extensive hands-on experience in oncology trial design and analysis; proficiency in SAS/R; strong communication and project management skills; ability to work independently and collaboratively. HighValue: oncology (RAS pathway), clinical trials, late-phase, regulatory interaction, statistical methodology development, cross-functional coordination. WorkSetup: onsite at Redwood City, CA, with a salary range of $211K-$264K, commensurate with experience.