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Manager Statistical Programming

Regeneron
September 06, 2026
Full-time
On-site
Cambridge, MA
Clinical Research and Development
Role: Manager, Statistical Programming supporting clinical studies across Regeneron's portfolio, leading programming deliverables from study initiation through regulatory approval and product launch. Responsibilities: oversee development and quality control of tables, listings, and figures; track project progress; serve as programming representative on multidisciplinary teams; collaborate with management on resource planning; participate in hiring and providing performance feedback. Requirements: Master's degree in a relevant discipline (Statistics, Computer Science, Mathematics, Engineering, Life Science) with 8-10 years (or 5+ years with relevant project/people management experience); proven experience leading programming for clinical studies; strong organizational and documentation skills in a regulated environment. Nice to have: SAS Certification. HighValue: support for clinical trials, regulatory submission, and product launch; experience within a therapeutic area or standard tools; work within GxP compliant environment. WorkSetup: onsite in Warren, NJ or Cambridge, MA; no explicit travel mentioned.