Senior SAS Statistical Programmer - Clinical Trials Lead

Cytel is seeking a Principal Statistical Programmer to work embedded with a global pharmaceutical client. You will lead SAS programming for complex clinical trial data and support CDISC SDTM/ADaM submissions with minimal supervision.

The role requires strong leadership, regulatory submission experience, and excellent communication. You will interact with CROs, FDA/EMA, and internal stakeholders, driving quality and timelines. #J-18808-Ljbffr