
This contract role involves serving as a Senior Statistical Programmer within the clinical research team at a pharmaceutical or medical device company in Irvine, California. The position focuses on developing and validating complex analysis datasets, tables, listings, and figures for regulatory submissions using Base SAS, SAS Macros, and CDISC standards. Key responsibilities include creating inspection-ready programming deliverables, collaborating with biostatisticians and data management teams, and independently managing project timelines. The role appeals to professionals seeking to work independently with minimal supervision while contributing to high-stakes clinical studies. It offers a structured on-site schedule with opportunities to apply advanced programming skills in a regulated environment.


















