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# Statistical Programmer

- **Company:** Katalyst Talent Agency
- **Location:** North Chicago, IL, United States
- **Experience:** Experienced
- **Contract:** Permanent contract
- **Skills:** Clinical Data Repository, Computer Programming, Data Governance, SAS (Software), Information Technology
- **Published:** October 27, 2026
- **Apply:** https://www.careerjet.com/job/us8c001ae8d7b3a1f44dc55c58596625d5/eaa

## About the Role

* Bachelor's Degree in statistics, computer science, or a similar quantitative field
 * 4+ years of clinical statistical programming experience within the pharmaceutical or related industry
 * Proficiency in SAS programming
 * Knowledge of CDISC data standards
 * Strong attention to detail and ability to work independently
 * Excellent problem-solving skills
 * Excellent verbal and written communication skills
 * Knowledge of regulatory requirements for clinical trials and drug development
 * Ability to work in a team environment and collaborate effectively with other stakeholders

## Description

* The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
 * The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting
 * Develop and validate SAS programs to support clinical trial data analysis and reporting
 * Create, maintain, and document SAS programming standards and procedures
 * Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met
 * Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency
 * The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry
 * Prepare datasets for analysis, including merging and cleaning data from various sources
 * Prepare and review tables, listings, and figures for clinical study reports
 * Ensure compliance with regulatory requirements and guidelines
 * Keep up to date with new SAS programming methods and software, as well as regulatory guidance