Senior Statistical Programmer

Regeneron Pharmaceuticals • Tarrytown, NY

447d • $92,500 - $151,100 • Hybrid

About The Position

The Senior Statistical Programmer at Regeneron Pharmaceuticals plays a crucial role in supporting clinical study teams by providing programming expertise in line with project strategies. This hybrid position requires the programmer to process, analyze, and store clinical study data according to established statistical analysis plans and regulatory requirements. The role involves leading programming efforts, ensuring data quality, and collaborating with multidisciplinary teams to facilitate the analysis and reporting of clinical trials, ultimately contributing to regulatory approvals and product launches.

Requirements

• MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field.
• 3+ years of programming experience in processing clinical trial data in the biotechnology, pharmaceutical, or health-related industry.
• Proficient in SAS programming (Base, Stat, Macro, graph) in a clinical data environment.
• Good understanding of relational database structures and reporting systems.
• Experience with standardization methodology and CDISC data standards.
• Strong understanding of biostatistics and pharmaceutical clinical development.

Nice To Haves

• Experience with R/R-Studio and MS-Excel.
• Ability to work independently and exercise judgment in interpreting and adapting procedures.

Responsibilities

• Lead and support programming and quality control of analysis datasets and TFLs for multiple studies.
• Represent PMX programming functions and coordinate activities with cross-functional teams, communicating timelines and milestones.
• Create, manage, and maintain programming specifications for analysis datasets using Regeneron tools and methodologies.
• Integrate data across studies to support Exposure-response, PopPK, and PopPKPD analyses.
• Create and validate electronic submission packages, including annotated CRFs and data export files.
• Provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval and product launch.

Benefits

• Health and wellness programs
• Fitness centers
• Equity awards
• Annual bonuses
• Paid time off

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Professional, Scientific, and Technical Services
• Education Level: Bachelor's degree