Associate Director, Biostatistics Clinical Late Stage

Role: Associate Director of Biostatistics leading statistical activities for late-stage oncology clinical trials, with a focus on RAS pathway inhibitors. Responsibilities: represent biostatistics on study and cross-functional teams, oversee statistical design, analysis, and reporting; develop analysis plans; collaborate with programming, data management, and clinical operations; contribute to regulatory documents and strategy; support publication efforts and stay updated on industry developments. Requirements: Ph.D. or M.S. in Statistics/Biostatistics; 5+ years (Ph.D.) or 8+ years (M.S.) experience in biotech/pharma, with hands-on experience in late-stage oncology trial design and analysis; proficiency in SAS and/or R; strong communication and project management skills; knowledge of ICH and regulatory standards. Preferred: experience in Phase 3 oncology trials. High-Value: oncology, RAS pathway, late-stage/Phase 3, statistical leadership, regulatory interaction, global development context. WorkSetup: on-site at Redwood City, CA; salary range $186K–$233K, with total rewards.