Clinical SAS Programmer

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• Engage directly with cross functional teams and contribute to high visibility clinical initiatives
• Work onsite in a collaborative setting that encourages knowledge sharing and technical excellence
• Lead programming efforts supporting clinical studies and regulatory deliverables
• Develop and validate SDTM and ADaM datasets in alignment with CDISC standards
• Produce high quality analysis outputs, including tables, listings, and figures for trials and publications
• Create, maintain, and optimize SAS macros and utilities to enhance programming efficiency
• Draft clear dataset specifications aligned with study protocols and analysis plans
• Partner with statisticians, data managers, and clinical teams to ensure accurate, timely outputs
• Manage multiple complex assignments and drive them to completion with minimal oversight
• Contribute technical expertise to problem solving, workflow enhancements, and process improvements.

• Grow your experience in a setting that values innovation, problem solving, and data accuracy
• 8+ years of clinical or statistical programming experience within pharma, biotech, or related industries
• Advanced SAS programming skills with demonstrated expertise in dataset creation and validation
• Deep familiarity with CDISC SDTM and ADaM standards
• Prior leadership experience supporting studies or overseeing programming deliverables
• Strong understanding of clinical trial data structures and regulatory expectations
• Excellent communication skills and ability to collaborate across cross functional teams
• Bachelor's degree in Statistics, Computer Science, Mathematics, or a relevant scientific discipline.

Mid-Senior level

Contract

Information Technology

Pharmaceutical Manufacturing