Clinical Data Programmer

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

Preferred Qualifications

Why Join Us?