Statistical Programmer (Hybrid)

Role: Statistical Programmer supporting clinical research in AbbVie's pharmaceutical R&D, primarily focused on analysis and reporting of clinical trial data. Responsibilities develop and validate SAS programs for creating ADaM datasets, Tables, Listings, Figures, and regulatory documentation consolidate heterogeneous data sources perform exploratory data analyses and visualizations collaborate with stakeholders in Statistics, Data Strategy, Medical Writing, and Regulatory Publishing Qualifications MS in Statistics, Computer Science, or related field with 0+ years (MS) or BS with 2+ years of experience practical SAS programming skills experience with pharmacokinetics and reporting clear communication skills Preferred pharma industry experience. High-Value role supports drug development, likely in phases involving clinical trial data analysis, with emphasis on regulatory compliance (CDISC standards); cross-functional collaboration across research teams. WorkSetup not specified; typically office-based or hybrid. #J-18808-Ljbffr AbbVie