Clinical Trials Programming Specialist

6 days ago


Tarrytown, New York, United States Regeneron Pharmaceuticals Full time
Key Responsibilities: As a Clinical Trials Programming Specialist at Regeneron Pharmaceuticals, you will be responsible for processing/analyzing/storing data from clinical studies according to a Statistical Analysis Plan, clinical pharmacology report requirement, Population PK/Population PK/PD analysis requirement, and programming specifications using internal standards and guidelines.

You will create, manage, and maintain programming specifications for analysis datasets using Regeneron tools and methodologies. Additionally, you will integrate data across studies in support of Exposure-response, PopPK, and PopPKPD analysis.

The successful candidate will have good SAS programming skills (SAS Base, Stat, Macro, Graph) in a clinical data environment and a strong understanding of relational database structure. They will also be able to take directives, work independently, exercise judgment in interpreting, modifying, and adapting procedures, practices, methods, etc. in accordance with existing policies and standards for application to specific problems or tasks.

We offer a competitive salary range of $92,500.00 - $151,100.00 annually.

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