Statistical Programming Specialist

2 days ago


Uxbridge, United Kingdom Regeneron Full time
In this dynamic and challenging role, you will be responsible for leading and supporting all programming activities per project strategies, working independently to implement and drive programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. You will collaborate with internal partnering functions, collaborators, and external functional service providers to ensure timely delivery of high-quality programming results. Additionally, you will develop and maintain programming documentations and specifications following programming standards and processes. With your strong background in SAS programming skills in a clinical data environment and excellent analytical skills, you will make a valuable contribution to Regeneron Pharmaceuticals' statistical programming team. We offer a comprehensive benefits package, including health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels. Apply now to take your first step towards living the Regeneron Way.

Key Requirements
  • A MS. (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline is required.
  • 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health-related industry is preferred.
  • Knowledge of other programming languages such as R, Python etc. is a plus.
  • A strong understanding of pharmaceutical clinical development, including statistical concepts, techniques, and clinical trial principles, is essential.


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