Discover Your Role
- 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
This Role Might Be For You If
- 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 across global, interdisciplinary teams; manage multiple priorities while maintaining quality
- You have a self-starter mindset and enjoy influencing, mentoring, and coaching
- You are energized by hands-on programming and people leadership
This Role Requires
- 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/coaching experience with junior programmers
- Education/experience: MS or BS in relevant fields (Statistics, Computer Science, Mathematics, Engineering, Life Science, or related) with 10+ years (12+ for BS) programming experience, preferably in clinical trial data; includes some project and people management experience
- Preferred: Knowledge of R or Python
Application: Apply now to take your first step toward living the Regeneron Way! Salary Range (annually): $150,500.00 - $245,500.00