Director, Statistical Programming

Role: Director of Statistical Programming, providing technical leadership across an indication/disease area with accountability for high-quality, efficient delivery of statistical analyses in clinical development. Responsibilities: lead programming activities, develop and implement strategies, oversee vendor and cross-functional team collaborations, drive process improvements, and manage personnel including hiring and performance management. Requirements: MS or BS with approximately 10+ or 12+ years of industry experience, proven leadership in statistical programming, experience in pharmaceutical drug development, and expertise in regulatory standards, clinical trial methodology, and programming standards. High-Value: focus on clinical trial programming within biopharma, including complex programs, regulatory compliance, and cross-functional influence. Collaboration with Therapeutic Area Heads and leadership team. Work setup: flexible, with potential for onsite, hybrid, or remote depending on role classification, with some travel. Emphasis on innovation, process optimization, and organizational leadership in a clinical research context.