Associate Director - Statistics, Specialty TA (Hybrid)

Role: Associate Director of Statistics leading statistical strategies in clinical development and product lifecycle management within AbbVie's biopharma portfolio, including immunology, oncology, and neuroscience. Responsibilities: provide expertise on trial design, statistical analysis, and regulatory submissions; develop protocols and analysis plans; collaborate with cross-functional teams (Clinical, Regulatory, Safety, GMA) to shape development strategies; mentor staff and supervise external statisticians; ensure regulatory compliance and contribute to scientific publications; act as liaison with CROs, academic institutions, and regulatory agencies. Requirements: MS with 10+ years or PhD with 6+ years in Statistics/Biostatistics; strong leadership skills; extensive industry knowledge of drug development in regulated environments; experience with submission processes preferred. High-Value: leadership in statistical methodology, cross-functional collaboration, regulatory engagement, and strategic input for clinical trial design in regulated biopharma settings, especially within immunology, oncology, and neuroscience. WorkSetup: not specified.