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 governanc...