Senior Statistical Programmer – SAS/CDISC for Submissions

A leading biotechnology company in Boston is looking for a Sr. Statistical Programmer to provide expert-level programming support for clinical trial data analysis and reporting. The ideal candidate will have over 6 years of experience with SAS, strong knowledge of CDISC standards, and a background in regulatory submissions. Responsibilities include developing and validating SAS programs, creating analysis datasets, and collaborating with cross-functional teams. Experience in oncology is preferred, and a strong commitment to quality and detail is essential. #J-18808-Ljbffr