> Markdown version of [/jobs/ext/4480677-manager-statistical-programming](https://www.wearedevelopers.com/jobs/ext/4480677-manager-statistical-programming). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Manager, Statistical Programming - **Company:** AbbVie Inc. - **Location:** North Chicago, IL, United States - **Experience:** Expert - **Salary:** $109,500.0 - **Contract:** Permanent contract - **Skills:** Data Definition Language, SAS (Software), Macros, Information Technology - **Published:** October 16, 2026 - **Apply:** https://www.businessworkforce.com/job.asp?id=3451626899&tx=KK7373FFQ&pt=1&aff=0B19D771-A501-4A5E-8338-2A822B784D54&utm_source=Job%20Feed&utm_medium=textkernel&utm_campaign=DE&utm_term=0B19D771-A501-4A5E-8338-2A822B784D54 ## About the Role * MS in Statistics, Computer Science or a related field with 8+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 10+ years of relevant experience. * Previous experience leading a team of statistical programmers. * In-depth understanding of SAS programming concepts and techniques related to drug development. * In-depth understanding of CDISC Standards. * In-depth understanding of the drug development process, including experience with regulatory filings. * Ability to communicate clearly both oral and written. * Ability to effectively represent the Statistical Programming Organization in cross functional teams. * Ability to accurately estimate effort required for project related programming activities. ## Description The Manager of Statistical Programming is a strategic role which guides a team of Statistical Programmers in the research and development of new pharmaceutical products. This role is directly responsible for leading the statistical programming activities for a compound/indication or therapeutic area in early development. The Manager of Statistical Programming must effectively interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations., * Leads the statistical programming activities for a compound/indication or therapeutic area in early development. * Leads a team of statistical programmers and manages the resource planning for assigned staff. * Ensures timely deliverables, that all quality processes are followed and consistency within the projects. * Develops and oversees the development of SAS programs for the creation of ADaM data sets following CDISC standards. * Develops and oversees the development of SAS programs for the creation of Tables, Listings and Figures. * Ensures consistency of ADaM data sets for individual studies and integrated data. * Creates documentation for regulatory filings including reviewers guides and data definition documents. * Leads the development of standard SAS Macros and participates in the development of standard operating procedures. * Provides oversight and mentoring of assigned Statistical Programmers, Statistical Analysts and Senior Statistical Analysts.