The Problem
As a research institution, Memorial Sloan Kettering writes hundreds of new clinical trials a year. Each of these trials needs an informed consent document, making it clear to trial participants what they are signing up for. We were asked to design a new authoring tool to make the process of writing these documents more streamlined.
Role & Team
I worked in partnership with one other designer, and an internal development team at Memorial Sloan Kettering.
This project is still in active development.
Early screen explorations
Consent writing workflow and proposed features of the authoring tool.