Clinical SAS Programmer

Responsibilities

• Engage directly with crossfunctional teams and contribute to highvisibility 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 highquality 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 problemsolving, workflow enhancements, and process improvements

Requirements

• Grow your experience in a setting that values innovation, problemsolving, 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 crossfunctional teams
• Bachelor's degree in Statistics, Computer Science, Mathematics, or a relevant scientific discipline