Statistical Programmer (Hybrid)
AbbVie
August 19, 2026
Remote friendly (North Chicago, IL)
United States
$65,500 - $125,500 USD yearly
Clinical Research and Development
The Statistical Programmer is an integral project team member in the research and development of new pharmaceutical products. Responsibilities include analysis and reporting of clinical trial data under the direction of a Senior Statistical Analyst.
Responsibilities:
- Create documentation for regulatory filings, including reviewer guides and data definition documents.
- Participate in the development of standard SAS macros.
- Consolidate heterogeneous data sources (clinical study databases, external databases, real-world data) to prepare analysis-ready datasets within a defined quality control process.
- Perform exploratory data analyses and visualizations with the clinical pharmacologist or pharmacometrician.
- Produce dynamic and static data visualizations to communicate quantitative analyses.
- Develop SAS programs to create ADaM datasets following CDISC standards.
- Develop SAS programs for creation of Tables, Listings and Figures.
- Validate ADaM datasets, and validate Tables, Listings and Figures.
- Create specifications for the structure of ADaM datasets for individual studies.
Qualifications:
- MS in Statistics/Computer Science (or related) with 0+ years relevant experience, OR BS (or related) with 2+ years relevant experience.
- Practical understanding of SAS programming and experience with pharmacokinetic (PK) analysis and reporting.
- Ability to communicate clearly orally and in writing.
Preferred Qualifications:
- Pharma experience.
Benefits (if eligible/eligible employees): paid time off (vacation, holidays, sick), medical/dental/vision insurance, 401(k), and eligibility for short-term incentive programs.
Responsibilities:
- Create documentation for regulatory filings, including reviewer guides and data definition documents.
- Participate in the development of standard SAS macros.
- Consolidate heterogeneous data sources (clinical study databases, external databases, real-world data) to prepare analysis-ready datasets within a defined quality control process.
- Perform exploratory data analyses and visualizations with the clinical pharmacologist or pharmacometrician.
- Produce dynamic and static data visualizations to communicate quantitative analyses.
- Develop SAS programs to create ADaM datasets following CDISC standards.
- Develop SAS programs for creation of Tables, Listings and Figures.
- Validate ADaM datasets, and validate Tables, Listings and Figures.
- Create specifications for the structure of ADaM datasets for individual studies.
Qualifications:
- MS in Statistics/Computer Science (or related) with 0+ years relevant experience, OR BS (or related) with 2+ years relevant experience.
- Practical understanding of SAS programming and experience with pharmacokinetic (PK) analysis and reporting.
- Ability to communicate clearly orally and in writing.
Preferred Qualifications:
- Pharma experience.
Benefits (if eligible/eligible employees): paid time off (vacation, holidays, sick), medical/dental/vision insurance, 401(k), and eligibility for short-term incentive programs.