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# Senior SAS Programmer

- **Company:** Greenfield Source
- **Location:** United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Training Data, Data Analysis, Coherent Remote File System (CRFS), Data Files, SAP (Applications), SAS (Software)
- **Published:** November 2, 2026
- **Apply:** https://www.careerbuilder.com/job-details/senior-sas-programmer--66c68264-b3d3-4a2e-a0e8-c3fc65e3b642

## About the Role

Statistical Analysis System (SAS), Statistics, SAP, Documentation, Statistical Analysis System (SAS), Data Sets, Pinnacle, Training Data Sets, Analysis Skills, Data Modeling

## Description

Be responsible for designing, developing, validating, and documenting SAS programs to generate summary tables, listings, graphs, and derived datasets as specified in the Statistical Analysis Plan (SAP)

 * Be responsible for creating and validating (through Pinnacle 21 or other tools) the Study Data Tabulation Model (SDTM) and the Analysis Data model (ADaM) datasets
 * Act as the core project team member and manage all statistical programming activities
 * Serve as the study programmer to design and specify the overall approach to a project's programming tasks
 * Provide statistical programming liaison with the client, statistician, and inputs for SAPs.
 * Create and maintain programming tracking documentation
 * Create, test, and maintain SAS programs for Clinical studies
 * Validate and transform datasets as per client assignment specifications
 * Validate tables, listings, and graphs as per client assignment specifications
 * Co-ordinate with the client and US-team for clarity of specifications, data issues, outliers, reviews, schedules, etc.
 * Be responsible for assisting statisticians in the development and review of SAPs and Programming specifications
 * Have an expert understanding of all current SDTM and ADaM domains
 * Be responsible for creating Case Report Tabulation Data Define Specification (CRTDDS) - Define.xml (metadata for the SDTM and ADaM)
 * Create annotated CRFs by following the SDTM
 * Create the Trial design Model (TDM)
 * Follow necessary departmental SOPs or Client specific SOPs and relevant regulatory guidelines (ex. ICH E9, E6 etc.)
 * Support assignments on single or multiple projects
 * Create standard macros and applications to improve the efficiency of the department
 * Be responsible for sharing better practices, guide and mentor less experienced Statistical programmers, peer-review programs written by less experienced statistical programmers
 * Be responsible for continuous development of own skills according to Individual Development Plan
 * Facilitate best practices in order to increase quality, efficiency, and productivity
*

Desirable Skills and Experience

 * Experience in SAS Programming is required
 * Be responsible for designing, developing, validating, and documenting SAS programs to generate summary tables, listings, graphs, and derived datasets as specified in the Statistical Analysis Plan (SAP)
 * Be responsible for creating and validating (through Pinnacle 21 or other tools) the Study Data Tabulation Model (SDTM) and the Analysis Data model (ADaM) datasets
 * Act as the core project team member and manage all statistical programming activities
 * Serve as the study programmer to design and specify the overall approach to a project's programming tasks
 * Provide statistical programming liaison with the client, statistician, and inputs for SAPs.
 * Create and maintain programming tracking documentation
 * Create, test, and maintain SAS programs for Clinical studies
 * Validate and transform datasets as per client assignment specifications
 * Validate tables, listings, and graphs as per client assignment specifications
 * Co-ordinate with the client and US-team for clarity of specifications, data issues, outliers, reviews, schedules, etc.
 * Be responsible for assisting statisticians in the development and review of SAPs and Programming specifications
 * Have an expert understanding of all current SDTM and ADaM domains
 * Be responsible for creating Case Report Tabulation Data Define Specification (CRTDDS)
 * Define.xml (metadata for the SDTM and ADaM) Create annotated CRFs by following the SDTM
 * Create the Trial design Model (TDM) Follow necessary departmental SOPs or Client specific SOPs and relevant regulatory guidelines (ex. ICH E9, E6 etc.)
 * Support assignments on single or multiple projects
 * Create standard macros and applications to improve the efficiency of the department
 * Be responsible for sharing better practices, guide and mentor less experienced Statistical programmers, peer-review programs written by less experienced statistical programmers
 * Be responsible for continuous development of own skills according to Individual Development Plan Facilitate best practices in order to increase quality, efficiency, and productivity
 * Desirable Skills and Experience Experience in SAS Programming is required