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# Clinical SAS Programmer

- **Company:** Katalyst Talent Agency
- **Location:** Omaha, NE, United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Databases, Graphical User Interface, Raw Data, SAS (Software), SAS/STAT, Macros, Information Technology, Data Management
- **Published:** October 26, 2026
- **Apply:** https://www.careerjet.com/job/us179860740b871abe607ea2006d5f7042/eaa

## About the Role

* MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 5 years.
 * Experience in providing statistical programming support to early and late phase clinical trials.
 * Excellent skills in SAS programming and statistical reporting.
 * Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements.
 * Familiarity with FDA and ICH regulations and guidelines.
 * Excellent problem-solving skills.
 * Good written and verbal communication skills and organizational and documentation skills.
 * Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc.
 * Ability to prioritize and multi-task effectively
 * Demonstrated positive attitude and the ability to work well with others.

## Description

* Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s)
 * Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets
 * Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements
 * Provides input in the design and development of case report forms and clinical databases
 * Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs
 * Programs quality checks for clinical study raw data and report the findings to Data Management
 * Provides input in the design and development of case report forms and clinical study databases
 * Reviews or author eCRF, SDTM and ADaM datasets specifications for datasets programming
 * Provides programming support for adhoc analysis
 * Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications)
 * Manages timelines and schedules of specific phases of projects with internal personnel and external vendors
 * Acts as lead programmer for a study
 * Reviews or validates statistical deliverables of vendors for assigned project(s)