Optimizing clinical trials: Sponsor/CRO cooperation; working together to enroll appropriate patients

Choosing the “right” CRO for your study and ensuring you get the “A” team or the team you were promised: and building a positive relationship with them
Clearly identifying who is responsible for each action item; especially items that are part of study start up (site ID, feasibility, site qualification) and how to proceed efficiently
Establishing realistic timelines and practicing constant communication to avoid timelines slipping
Keeping patients in mind when designing the protocol
Utilizing updated technology: A look at a recently adopted eISF system and potentially adopting a RBQM system
Using sites with a diverse population and promising constant communication with them
Sending an initial budget template early on to help streamline the budget process and identify sites that may not fit within the study budget early on.