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.