Clinical SAS Programmer

Katalyst Healthcares & Life Sciences

10 months ago

Not enough detail in this posting to match

Responsibilities:

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.

Requirements:

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.

Clinical SAS Programmer · Katalyst Healthcares & Life Sciences