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Hybrid opportunity at
AbbVieStatistical Programmer (Hybrid)
AbbVie seeks a Statistical Programmer to join its research and development organization on a hybrid schedule. This position acts as a key project team member supporting…
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About this role
Statistical Programmer (Hybrid) at AbbVie is a full-time role. Work arrangement: Hybrid. Location: Not specified. No salary is shown in this listing. It was posted on Oct 1, 2026. This listing is paused and not taking applications at the moment.
Job Description
AbbVie seeks a Statistical Programmer to join its research and development organization on a hybrid schedule. This position acts as a key project team member supporting the creation of novel pharmaceutical products. The organization focuses on discovering and delivering innovative therapeutics to address serious current health problems and future medical challenges across therapeutic fields such as oncology, immunology, neuroscience, and the Allergan Aesthetics portfolio.
This role suits professionals with a background in statistics or computer science who want to apply their programming skills to clinical trial data analysis and reporting. Under the guidance of a Senior Statistical Analyst, the chosen candidate will collaborate with multiple internal stakeholders including statistics, clinical data strategy and operations, medical writing, regulatory publishing, and development operations.
Daily work centers on gathering disparate data sources to build analysis-ready datasets, writing SAS programs for ADaM datasets and output displays, conducting validation tasks, and generating regulatory documentation. The position also involves building data visualizations and interacting with pharmacologists or pharmacometricians for exploratory analyses. Eligible staff may participate in short-term incentive plans and receive standard employee benefits. AbbVie is an equal opportunity employer committed to ethical practices and community service.
Responsibilities
- Prepare regulatory filing documentation such as reviewer guides and data definition documents
- Contribute to the creation of standard SAS macros
- Consolidate multiple data sources like clinical databases and real-world data into analysis-ready datasets
- Conduct exploratory data analyses and create visualizations alongside clinical pharmacologists or pharmacometricians
- Produce static and dynamic data visualizations for quantitative assessments
- Write SAS programs to generate ADaM datasets adhering to CDISC standards and tables, listings, and figures
- Validate ADaM datasets alongside tables, listings, and figures
- Draft specifications for individual study ADaM dataset structures
Requirements
- Demonstrated practical understanding of SAS programming
- Experience with pharmacokinetic analysis and reporting
- Clear oral and written communication skills
Qualifications
- Master of Science degree in Statistics, Computer Science, or a related discipline with zero or more years of relevant experience
- Bachelor of Science degree in Statistics, Computer Science, or a related discipline with at least two years of relevant experience
- Prior pharmaceutical industry experience
Core Skills
Benefits
- Paid time off covering vacation, holidays, and sick leave
- Medical, dental, and vision insurance coverage
- Participation in a 401(k) plan
- Eligibility for short-term incentive programs
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
What is the remote work policy for this position?
The role is structured as a hybrid position.
What education and experience are required to apply?
Applicants need either a Master of Science in Statistics, Computer Science, or a related field with zero-plus years of experience, or a Bachelor of Science in the same fields with two-plus years of relevant experience.
What is the specific salary for this role?
The exact salary is not stated in the job posting, though eligible employees may participate in short-term incentive programs and receive a comprehensive benefits package.
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