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As a Senior Associate in Statistical Programming, you will create quality outputs for clinical trials, develop and validate CDISC-compliant datasets, maintain project documentation, and ensure timely delivery of programming deliverables. You are expected to contribute to project objectives, undergo regulatory training, and lead programming activities.

The role involves ensuring quality in statistical outputs, developing and maintaining programming standards, and guiding documentation for clinical studies. The individual will be responsible for timely delivery, developing CDISC compliant datasets, and mentoring programming teams while maintaining professionalism and quality under regulatory compliance.