• Lead programming activities for oncology clinical trials across multiple studies. • Develop, validate, and maintain SDTM and ADaM datasets following CDISC guidelines. • Oversee production of Tables, Listings, and Figures (TLFs) for study reporting and submissions. • Provide SAS programming expertise to support complex data derivations and analyses. • Review and ensure traceability, consistency, and quality of all programming deliverables. • Act as programming lead for assigned studies, managing timelines and deliverables. • Work closely with Biostatistics, Data Management, Medical Writing, and Regulatory Affairs. • Coordinate with CROs and external vendors, ensuring compliance, quality, and adherence to client programming standards. • Support integrated analyses including ISS/ISE. • Prepare submission-ready programming outputs and documentation, including define.xml, annotated CRFs, and reviewer guides. • Ensure all programming meets regulatory requirements (FDA, EMA, PMDA). • Contribute to responses for regulatory queries and data requests.