Science 37 is seeking a Clinical Study Design Manager to define eSource platform specifications and oversee the full design-to-implementation lifecycle. You will coordinate offshore build teams, ensure quality standards, and partner with clinical operations to align protocols with data capture requirements.
The role requires 3+ years in clinical research design (CRF/ePRO) and 2+ years with CRIO platforms. Strong communication and leadership are essential for success in a fast-paced, global team.
#J-18808-LjbffreSource Platform Design Lead for Clinical Studies in northern at Unknown Company
This position is listed as full time and onsite.