Principal Statistical Programmer - Internal Medicine
Build our future together:
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will provide programming leadership and support for processing clinical trial data, designing and testing program logic while ensuring consistent, high-quality documentation, all while collaborating with a multidisciplinary study team to support analysis and reporting through regulatory approval and beyond.
This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
When & where:
- Location: Warren, NJ or Cambridge, MA
- Work model/flexibility: onsite
Discover your role:
- Support or lead programming and quality control of analysis datasets, tables, listings, and graphs
- Coordinate activities and communicate shifting timelines and milestones to the study team
- Create and maintain programming specifications for analysis datasets across studies
- Support creation and validation of submission requirements, including annotated CRFs and define documents
- Work within a multidisciplinary study team to provide timely, quality support through regulatory approval and launch
- Provide programming support for presentations and statistical ad hoc requests, assisting with more complex data as needed
- Participate in department working groups, contributing to tool development and process improvement
- Design and test program logic independently, maintaining documentation in a regulated environment
This role might be for you if you:
- Enjoy working independently while staying closely connected to a broader study team
- Communicate clearly and proactively, especially around shifting timelines
- Take pride in accuracy and consistency when documenting and maintaining code
- Think analytically and enjoy solving programming and data challenges
- Stay curious about process improvement and enjoy contributing ideas to working groups
- Adapt comfortably to ad hoc requests and evolving priorities from senior leadership
- Bring attention to detail and a quality mindset to regulated work
This role requires:
- Master's degree with 3+ years of relevant experience
- Proven programming experience supporting clinical study data and analysis deliverables
- Strong documentation and quality control skills within a regulated environment
- Experience collaborating within a multidisciplinary study team
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