Key Responsibilities Develop, validate, and maintain ADaM datasets , TLFs , and other analytical outputs for clinical trials. Support Oncology studies by ensuring accuracy, consistency, and regulatory compliance in all programming deliverables. Contribute to ISS/ISE activities , including dataset integration, analysis, and documentation. Work closely with statisticians, data managers, and clinical teams to ensure timely and quality delivery. Assist in regulatory submissions and RTQs , providing clear, traceable, and compliant programming outputs. Collaborate in an agile environment , participating in sprint meetings, planning, and continuous improvement discussions. Work with internal tools and platforms, including GSK-specific tools , following established standards and governance. Troubleshoot data/programming issues and propose process enhancements. Ensure adherence to CDISC standards, good programming practices, and audit-ready documentation. Required Skills & Qualifications Profic...