What are the responsibilities and job description for the Clinical SAS Programmer position at Katalyst CRO?
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.
- 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.