Merck is seeking an Senior Statistical Programmer to support late-stage clinical development and regulatory submissions. You will lead SAS programming across trials, develop analysis datasets, and ensure quality and compliance with global standards.
The role requires extensive experience in SAS, CDISC/ADaM, and collaboration with cross-functional teams. A strong background in data management and statistical methodology is essential.
#J-18808-LjbffrRemote Global Lead Statistical Programming in rahway at Unknown Company
This position is listed as full time and onsite.