Job Description

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...

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