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Sr. Statistical Programmer

Glaukos Corporation
United States, California, San Clemente
Sep 22, 2025

What You'll Do:

The Senior Statistical Programmer generates tables, listings and graphs to support statistical analyses of data for clinical studies, regulatory submissions and publications. This position requires a good understanding and ability to provide datasets using current industry standards including Clinical Data Interchange Standards Consortium (CDISC) Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM).



  • Review key study documents produced by other functions (protocols, statistical analysis plans [SAPs], TFL shells, case report forms) and interact with
  • Statisticians and other clinical team members to ensure programming requirements are understood.
  • Follow SAPs, develop specifications and execute derivation algorithms for
  • analysis dataset production.
  • Follow the SDTM and ADaM Implementation Guide to develop specifications, create programs to produce CDISC-compliant SDTM and ADaM datasets and define.xml files.
  • Generate tables, figures, and listings, (TFLs) in accordance with the SAP and TFL shells to support analyses using Base SAS, SAS Macro, SAS/STAT,
  • SAS/GRAPH, or other statistical graphics technology.
  • Create and maintain integrated analysis datasets including closed and ongoing studies.
  • Validate SAS programs, macros, datasets, and TFL output generated by other Programmers.
  • Develop or assist in the development of departmental processes and procedures.
  • Other duties as assigned.


How You'll Get There:



  • Experience working in Pharmaceutical/ Biotechnology/CRO industry as a
  • Statistical Programmer is required (>= 3 years with MS
  • degree; >=5 years with BS degree).
  • High proficiency in SAS programming and Macro development
  • Experience working with CDISC SDTM and ADaM compliant data sets
  • Experience with regulatory submissions and creating Define.XML.
  • Knowledge of statistics and the drug development process
  • In-depth knowledge of FDA/ICH guidelines and industry/technology standard
  • practices
  • Knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs
  • Capable of critical thinking and independently identifying issues in existing programs
  • Solid verbal and written communication skills
  • Bachelor's /Master's Degree in Statistics, Mathematics, Computer Science, or other related discipline is required; Master's degree is preferred

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