Principal Statistical Programmer - Genetic Medicines
$109.9k - $179.3kRegeneron Pharmaceuticals, Inc.
Regeneron seeks a Principal Statistical Programmer to lead clinical trial data programming and quality control activities supporting regulatory submissions and study launches. The role involves designing analysis datasets, specifications, and validation documents while collaborating with multidisciplinary teams across the clinical portfolio.
Responsibilities
- Lead programming and quality control of analysis datasets, tables, listings, and graphs
- Create and maintain programming specifications for analysis datasets across multiple studies
- Design, test, and independently validate program logic while maintaining regulated documentation
- Support creation and validation of regulatory submission requirements including annotated CRFs
- Provide statistical programming support for presentations, ad hoc requests, and timely study team needs
Requirements
- Master's degree with 3+ years of clinical study programming experience
- Proven ability to process clinical trial data and create analysis deliverables
- Strong documentation and quality control skills in regulated environments
- Experience collaborating within multidisciplinary study teams
- Analytical mindset with attention to detail and accuracy in code maintenance
Compensation: $109,900–$179,300 annually
Vacancy posted 1 day ago
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