Clinical SAS Programmer

Job Title

Engage directly with cross-functional teams and contribute to high-visibility clinical initiatives

Work on-site 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