Statistical Analyst - ADaM Programming (Hybrid)

Role: Statistical Analyst supporting clinical trial data analysis and reporting in pharmaceutical R&D, primarily focusing on routine activities with supervision for complex tasks. Responsibilities: lead statistical programming for studies, create documentation for regulatory submissions, develop and validate SAS programs for ADaM datasets, Tables, Listings, Figures, and data visualizations. Collaborate with Statistics, Clinical Data Strategy & Operations, and Development Operations. Requirements: MS in Statistics, Computer Science, or related field with 2+ years (MS) or BS with 4+ years relevant experience; practical SAS programming experience in drug development; knowledge of CDISC standards and clinical trial processes. Preferred: experience supporting efficacy analyses across phases and therapeutic areas. High-Value: involvement in clinical trial data analysis, ADaM dataset creation, and regulatory documentation within pharmaceutical R&D. WorkSetup: not specified.