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# Senior Manager, Statistical Programming - Hematology

- **Company:** Regeneron
- **Location:** Warren, NJ, United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Clinical Data Repository, Computer Programming, Python (Programming Language), SAS (Software), Information Technology, Programming Languages
- **Published:** October 8, 2026
- **Apply:** https://dejobs.org/x/x/91108E951366467FBBDEDDE7FA04E1E8/job/

## About the Role

* MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline, with 10+ years (12+ for BS) of programming experience - preferably in clinical trial data within biotechnology, pharmaceutical, or health-related industries, including some project and people management experience
 * Advanced SAS programming expertise in a clinical data environment
 * Strong understanding of clinical trial principles and regulatory submission requirements
 * Proven ability to lead global, cross-functional teams
 * Experience managing multiple concurrent projects and priorities
 * Demonstrated mentoring or coaching experience with junior programmers
 * Preferred/nice to haves:Knowledge of additional programming languages such as R or Python

## Description

* Lead programming support across multiple studies, ensuring timely, high-quality deliverables
 * Coordinate programming documentation and specifications, following established standards
 * Champion company values through excellence, collaboration, and accountability
 * Communicate proactively with study and project teams to clarify requirements and guide programmers
 * Lead submission-ready programming deliverables for global regulatory authority filings
 * Drive department goals and serve as a subject matter expert on key topics
 * Guide the development of direct reports through goal-setting, coaching, and mentoring
 * Contribute to hiring by screening and interviewing programming candidates
 * You bring advanced SAS skills honed in a clinical data environment, ideally across multiple therapeutic areas
 * You understand pharmaceutical clinical development, statistical concepts, and regulatory submission requirements
 * You collaborate naturally across global, interdisciplinary teams
 * You juggle multiple projects and priorities without losing sight of quality
 * You solve problems with initiative, creativity, and a self-starter mindset
 * You enjoy influencing, mentoring, and coaching others toward strong results
 * You lead with accountability and hold yourself to a high bar
 * You're energized by both hands-on programming work and people leadership