• Develop, validate, and maintain SDTM and ADaM datasets using R following CDISC standards. • Support TLF (Tables, Listings, Figures) generation in R or SAS as needed. • Write efficient, reproducible, and well-structured R scripts for clinical data analysis and reporting. • Collaborate with statisticians, data managers, and clinical teams to understand programming requirements. • Perform QC checks, reconcile data issues, and ensure deliverables meet regulatory expectations (e.g., FDA, EMA). • Contribute to programming workflows, documentation, and version control best practices. • Support automation initiatives and R-based pipeline development. • Utilize SAS for legacy studies or where SAS support is required.