Statistical Programmer: CDISC/SAS for Submissions

A clinical research organization is seeking a skilled Statistical Programmer to manage and analyze clinical trial data. In this role, you will develop SAS programs, guarantee quality of statistical outputs, and support regulatory submissions. The ideal candidate holds a Bachelor's degree in a scientific discipline and has experience with SAS. You will work in a mid-senior level position that offers a contract employment type, collaborating with a team to ensure the highest quality of analysis and compliance with standards. #J-18808-Ljbffr