Data Analysis Programmer

3 days ago

India Astek Full time

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. Troubleshoot data/programming issues and propose process enhancements. Ensure adherence to CDISC standards, good programming practices, and audit-ready documentation. 4-14 years of Industrial experience ~ Proficiency in R programming ~(Solid experience in SAS programming , especially in a clinical/biostatistics environment. ~ Hands-on expertise in ADaM dataset development and TLF programming . ~ Good understanding of CDISC standards and clinical trial data flow. ~ Advanced or Expert-level R Programming skills. Experience working on Oncology therapeutic area studies. Exposure to ISS/ISE , submission workflows, and regulatory interactions (e.g., Practical understanding of agile ways of working (Scrum/Kanban). Prior experience using or supporting GSK tools and platforms . Opportunity to work on impactful Oncology research with global teams Collaborative, agile work culture Exposure to end-to-end statistical programming lifecycle and regulatory submissions

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