SAS Programmer III

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day-to-day functions. Organizations need to reduce training and labor costs while requiring the best "talent" for the job.

• Bachelor's or Master’s degree in Computer Science, Statistics, Mathematics, Life Sciences, or other relevant scientific subjects.
• 8+ years of clinical research and development statistical programming experience using SAS.

Responsibilities include performing all SAS programming required for clinical trial analysis and reporting, ensuring activities are conducted according to sponsor requirements, and collaborating with Biostatistics and Data Management departments. The role involves leading programming efforts for large complex studies, reviewing CRF design, designing and reviewing database structures, and writing, testing, and validating SAS programs for analysis datasets, TLGs, and reports. The programmer will also write CDSIC standard dataset specifications, create SDTM and ADaM datasets, and develop macros and utilities at the department, product, and study levels.

Acts as primary programmer for CSR tables, listings, and figures, and validates secondary programs. Requires 5-7 years of experience, strong SAS skills, extensive CDSIC standards experience, and familiarity with FDA/EMEA trial submissions and drug development processes.