Associate Director Statistical Programming - Pharmacometrics
Regeneron Pharmaceuticals, Inc.
Responsibilities
- Lead programming and quality control of analysis datasets across multiple projects
- Create, manage, and maintain programming specifications using Regeneron tools
- Integrate data across studies for exposure-response and population pharmacokinetics analysis
- Plan and validate electronic submission requirements for regulatory filings
- Support multidisciplinary study teams on analysis and reporting through regulatory approval
Requirements
- Master's degree in Statistics, Computer Science, Mathematics, Engineering, or Life Science
- 10+ years programming experience in clinical trial data processing
- Expert SAS programming skills including Base, Stat, Macro, and Graph modules
- Strong knowledge of CDISC data standards and standardization methodology
- Comprehensive understanding of biostatistics and pharmaceutical clinical development
- Experience with relational databases and data delivery applications
- Project and people management experience preferred
Vacancy posted 6 days ago
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