Senior Statistical Programmer: SAS/CDISC & Submissions

A leading oncology firm located in Boston, Massachusetts, is seeking a Sr. Statistical Programmer to deliver expert programming support for clinical trial data analysis. The ideal candidate will have at least 6 years of experience with SAS, strong knowledge of CDISC standards, and the ability to work independently. Responsibilities include developing SAS programs for regulatory submissions and collaborating across departments. The company offers a competitive salary, annual bonus, and comprehensive benefits package. #J-18808-Ljbffr