Associate Director - Statistics, Specialty TA (Hybrid)

Role: Associate Director of Statistics leading statistical strategies for clinical development and lifecycle management of biopharma projects, focusing on regulatory submissions, trial design, analysis, and reporting. Responsibilities: provide statistical expertise across clinical trials, collaborate with cross-functional teams (Clinical, Regulatory, Patient Safety, Medical Affairs), develop protocols and analysis plans, mentor staff, ensure regulatory compliance, and represent the department externally. Requirements: MS with 10+ years or PhD with 6+ years in Statistics/Biostatistics; strong industry knowledge, leadership skills, experience managing cross-cultural teams, and understanding of drug development in regulated environments. Preferred: PhD, submission experience. High-value: extensive biotech industry experience, regulated environment expertise, and collaboration with external partners like CROs and regulatory agencies. Work setup and travel specifics are not specified.