Associate Director - Statistics, Specialty TA (Hybrid)

Role: Associate Director, Statistics, providing statistical leadership for clinical development and lifecycle management of biopharma projects, focusing on regulatory submissions and scientific research. Responsibilities: lead statistical design, analysis, and reporting, develop protocols and analysis plans, collaborate with multidisciplinary teams to create development strategies, mentor staff, ensure regulatory compliance, and represent statistics in external collaborations. Qualifications: MS with 10+ years or PhD with 6+ years in Statistics or Biostatistics; strong industry experience with drug development in regulated environments; leadership skills and experience managing cross-cultural teams. Preferred: PhD, regulatory submission experience. High-Value: expertise in statistical methodology, regulatory interactions, and development lifecycle; experience in clinical trials, regulatory submissions; focus on immunology, oncology, neuroscience therapeutic areas. Work setup: not specified, but likely office-based with cross-functional engagement.