Clinical trial feasibility – it’s a standard part of recruitment planning and essential for predicting enrollment success. Yet so often it’s easy to get wrong, putting timelines and budget at risk. And whether that’s because there’s too great a focus on quantitative factors – such as volume of patients or number of competing studies – it’s clear that study sponsors and sites can benefit from an enhanced approach. This session will present attendees with a new perspective on feasibility models, featuring an approach that combines quantitative and qualitative characteristics to help accurately ascertain a site’s probability of enrollment success. This session will introduce qualitative factors – such as investigator enthusiasm for the investigational compound and study coordinator motivation / bandwidth – to the feasibility conversation.
This course requires enrollment in Tufts CTSI iLearn.
Enroll in course here.