Statistical Analyst - ADaM Programming (Hybrid)

Role: Statistical Analyst supporting clinical trial data analysis and reporting within AbbVie's R&D. Responsibilities: lead routine statistical programming activities, develop and validate SAS programs for ADaM datasets, Tables, Listings, and Figures; create regulatory documentation such as reviewer guides and data definitions; produce data visualizations; support validation processes. Requirements: MS in Statistics, Computer Science, or related field with 2+ years of experience, or BS with 4+ years; practical SAS programming skills; experience with ADaM data standards; understanding of CDISC standards and drug development processes; strong communication skills. Preferred: ability to support efficacy analyses across phases and therapeutic areas. HighValue: pharmaceutical clinical trials, SAS programming, ADaM data standards, regulatory documentation, experience in drug development. WorkSetup: not specified; based at AbbVie's discretion.