Principal Statistical Programmer - Genetic Medicines

$109.9k - $179.3k

Regeneron 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

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Vacancy posted 2 days ago

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