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.
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