Apply your SAS/ADaM programming expertise to advance life-changing clinical trials at Syneos Health, a global biopharmaceutical CRO, earning $110k–$150k/yr. As Principal Statistical Programmer, you'll architect complex data solutions for Phase II–IV trials in a senior remote role with technical depth and impact.
You'll design and validate CDISC ADaM and SDTM datasets for regulatory submissions, write production SAS code that meets FDA 21 CFR Part 11 standards, perform statistical quality reviews and troubleshoot programming issues, mentor junior programmers on best practices and standards, and collaborate with biostatisticians and medical monitors on trial analysis.
You need 10+ years of SAS programming experience in clinical trials with deep expertise in ADaM, SDTM, and CDISC standards. A bachelor's degree in statistics, computer science, or a related field is required. SAS Certified Professional status and previous FDA submission experience are highly valued.
