Yuxi Global powered by Veritas Automata
Yuxi Global (powered by Veritas Automata) is a leading people and technology force multiplier dedicated to empowering businesses in achieving their digital goals since 2005. We specialize in providing comprehensive solutions, including turnkey enterprise-grade application, managed development teams and strategic consulting via our Veritas Automata Services Team, tailored to meet the unique requirements of our clients. We are headquartered in the United States and operate with a robust team of over 150 skilled IT professionals located strategically in North and South America, including the United States, Colombia, Mexico, Brazil, and Costa Rica.
201 - 500 employees
Statistical Programmer
October 31
Yuxi Global powered by Veritas Automata
Yuxi Global (powered by Veritas Automata) is a leading people and technology force multiplier dedicated to empowering businesses in achieving their digital goals since 2005. We specialize in providing comprehensive solutions, including turnkey enterprise-grade application, managed development teams and strategic consulting via our Veritas Automata Services Team, tailored to meet the unique requirements of our clients. We are headquartered in the United States and operate with a robust team of over 150 skilled IT professionals located strategically in North and South America, including the United States, Colombia, Mexico, Brazil, and Costa Rica.
201 - 500 employees
📋 Description
• Perform statistical programming activities to support data analysis, interpretation, and regulatory submissions. • Develop, validate, and maintain SDTM and ADaM datasets in accordance with CDISC standards. • Generate high-quality Tables, Listings, and Figures (TFLs) per SAP and study requirements. • Prepare and maintain programming deliverables including dataset specifications, documentation, reviewer guides, and QC records. • Mentor and train junior programmers; help elevate programming standards, workflows, and best practices. • Collaborate across biostatistics, data management, clinical operations, and project management to ensure seamless execution of deliverables. • May serve as Programming Lead on assigned studies.
🎯 Requirements
• Experience as a statistical programmer within clinical trials (pharma, biotech, or CRO). • Demonstrated proficiency in TFL programming. • Strong command of CDISC SDTM and ADaM standards and submission practices. • Experience preparing regulatory submission documentation and supporting data review. • High attention to detail, structured communication style, and strong documentation discipline. • Bachelor’s degree in statistics, computer science, life sciences, mathematics, or related field.
🏖️ Benefits
• Employees can work remotely
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