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# SAS Programmer III

- **Company:** Katalyst Talent Agency
- **Location:** Durham, NC, United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Clinical Data Repository, Data Validation, SAP (Applications), SAS (Software), System Testing, Information Technology, Data Management
- **Published:** October 27, 2026
- **Apply:** https://www.careerjet.com/job/us49afbeebc28534eab372fc1480f7a9e5/eaa

## About the Role

* BS or above in computer science/statistics with at least 5 years of SAS experience in major pharma or CRO.
 * Develop SAS coding for generating SDTM, ADaM datasets and TLFs to support clinical study analysis
 * Proficient computer skills across multiple applications and OS environments

## Description

* Review and ensure accurate and high-quality statistical programming deliverables from CRO.
 * Perform generation, validation and QC/QA of SDTM, ADam and TFL output in accordance with SOPs, SOIs, and guidance documents.
 * Create and maintain specifications as per SDTM/ADaM standard and study SAP.
 * Define and create ad-hoc reports and listings for clinical teams.
 * Develop, implement and maintain SAS programming standards.
 * Builds/tests programs for Data Validation, Derivation, and Data Reports to identify inconsistencies and support data review efforts, as necessary.
 * Verifies completeness of relevant study deliverables prior to release from the group Maintains all required study documentation.
 * Consults and provides input into system validation efforts including tool maintenance activities.
 * Ensure CRF meets the guidelines of the protocol and check for consistency and adequacy.
 * Work in tandem with Biostatistics and Data Management member on various clinical projects.
 * Review CRF annotations and data specifications.
 * Perform quality control on final reports.
 * Develop SAS coding and table templates for preparing, processing and analyzing clinical data.
 * Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues.
 * Perform clinical study report and/or exploratory analysis for oncology clinical study
 * Perform validation of ADaM datasets and TLFs per SAP.
 * Effectively review and comment on vendor programming deliverables and help resolve technical difficulties.