Responsibilities
Develop and validate SAS programs for clinical data conversions, analysis datasets, and study tables, figures, and listings (TFLs), following CDISC or customer requirements. Create programming specifications and best practices, review programming outputs, and potentially manage project scope, timelines, budgets, and resources while mentoring team members and interacting with customers.
Requirements
Requires a bachelor’s degree in statistics, computer science, or a life science discipline and 6–8 years of statistical programming experience on clinical trials. Candidates should have strong TFL programming and CDISC SDTM/ADaM experience, submission documentation knowledge, attention to detail, and excellent communication skills.
