Description
The Statistical Programmer Contractor develops, validates, and maintains SAS programming deliverables for clinical study analysis and reporting. The role creates SDTM and ADaM specifications, datasets, tables, listings, figures, and supporting documentation; performs quality control and validation; collaborates with biostatistics and other study teams; resolves data and output issues; and maintains audit-ready documentation. The position requires a bachelor’s degree, at least 10 years of relevant statistical programming experience in the pharmaceutical, biotechnology, or CRO industry, strong SAS and clinical trial knowledge, and eligibility to work in the United States without visa sponsorship.
