Associate Director, Biostatistics

Role: Biostatistician supporting clinical development in Summit’s oncology trials, including Phase 3 studies in NSCLC and colorectal cancer. Responsibilities: develop statistical analysis plans, sample size calculations, review study documents, perform data analysis, collaborate on database design, and contribute to regulatory submissions and publications. Requirements: Ph.D. in Statistics/Biostatistics or MS with extensive industry experience; 6+ years (Ph.D.) or 8+ years (MS); proficiency in SAS, R; understanding of clinical trial processes, GCP, ICH, FDA guidelines. High-Value: oncology (NSCLC and CRC), Phase 3 trials, regulatory compliance, biomarker and safety analysis, collaboration with clinical operations and CROs. WorkSetup: not specified; salary range $190,000–$210,000; emphasis on biopharma research in immuno-oncology.