Senior Biostatistician

Statistical Programming OpportunityWe are seeking a skilled Statistical Programmer to join our team. As a key member of our statistical programming department, you will be responsible for developing and maintaining ADaM datasets, TLFs, and other analytical outputs for clinical trials.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.Troubleshoot data programming issues and propose process enhancements.Ensure adherence to CDISC standards, good programming practices, and audit-ready documentation.Requirements:4-14 years of industrial experience.Proficiency in R programming.Intermediate candidates with strong learning intent and ability to upskill quickly will also be considered.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.Strong problem-solving skills, attention to detail, and ability to work in cross-functional teams.Benefits:Opportunity to work on impactful Oncology research with global teams.Continuous learning and upskilling environment.Collaborative agile work culture.Exposure to end-to-end statistical programming lifecycle and regulatory submissions.