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Associate Director Statistical Programming

Regeneron
August 31, 2026
Full-time
Remote friendly (Warren, NJ)
Worldwide
Clinical Research and Development
Role: Associate Director, Statistical Programming leading a team within Regeneron's biopharma research, supporting therapeutic programs in a hybrid work setting. Responsibilities: oversee statistical programming activities, develop departmental standards, guide study teams, ensure deliverable quality, and mentor staff; contribute to process improvements. Requirements: Master's degree in a relevant field; 10+ years of clinical programming experience with advanced SAS skills; proven project and team management across global, interdisciplinary teams; strong understanding of pharmaceutical development and regulatory submission processes. HighValue: expertise in clinical data environments, therapeutic area knowledge, leadership in program management, and experience supporting regulatory filings. WorkSetup: hybrid Warren, NJ; no specific travel indicated.