Director, Statistical Programming
Bristol Myers Squibb
October 1, 2026
Full-time
Remote friendly (Madison, NJ)
Worldwide
Clinical Research and Development
Role: Director, Statistical Programming at Bristol Myers Squibb, providing technical leadership and strategic oversight for statistical programming activities across indication/disease areas. Objectives include ensuring high-quality, timely delivery of programming projects, leading process improvements, and supporting clinical development in areas like cell therapy or biologics. Responsibilities involve managing teams of leaders, developing and executing programming strategies, and collaborating with cross-functional stakeholders such as clinical, regulatory, and data teams. Key tasks include overseeing project execution, recruiting and retaining talent, and implementing innovative programming technologies. Requirements: MS or BS with 10+ years of industry experience in pharmaceutical or biotech drug development, proven expertise in clinical trial programming, process transformation, and team leadership. High-value specifics include experience with biologics, cell/gene therapies, or advanced modalities; familiarity with global regulatory standards and GxP compliance; and involvement in phases from IND to post-market. The role reports to Therapeutic Area Heads, with a focus on strategic execution and operational excellence. Work setup may vary between onsite, hybrid, or remote, based on business needs, with some travel expected.