Director, Statistical Programming
Bristol Myers Squibb
September 03, 2026
Full-time
Remote friendly (Madison, NJ)
Worldwide
Clinical Research and Development
Role: Director of Statistical Programming leading portfolio delivery within Bristol Myers Squibb's clinical development. Main objectives include providing strategic technical leadership, ensuring high-quality statistical programming execution, and driving process improvements across indications/disease areas. Responsibilities encompass managing statistical programming activities, developing indication-specific strategies, overseeing recruitment and retention, and supporting complex clinical project teams and vendors to meet regulatory standards. The role involves proactive engagement in cross-functional collaborations, influencing process enhancements, and contributing to leadership vision. Requirements: MS or BS degree with approximately 10+ years (MS) or 12+ years (BS) of industry experience; proven track record in clinical programming, process transformations, talent management, and knowledge of drug development, clinical trial methodology, and regulatory guidance. High-value specifics include extensive exposure to pharmaceutical R&D, clinical trial analysis, and regulatory compliance, with responsibilities spanning GxP practices. The position reports to Therapeutic Area Heads, supporting indication/disease area strategies, and involves a leadership role managing a team of managers and individual contributors. Work setup includes hybrid or onsite options, with travel as needed. The role emphasizes leadership, innovation, and operational excellence in statistical programming within a global biopharma R&D environment.