Clinical Protocol Development Series – Day 2

The goal of this two-day series is to provide researchers with knowledge, tools, and resources to aid in the development of a scientific protocol for a clinical research study. Both sessions will begin at 9:00 AM and a question-and-answer session will follow each presentation.

On the second day of the series we will take a “deeper dive” into clinical study design, statistics, and their impact on clinicaltrials.gov reporting:
– Clinical Protocol Study Design – aims, objectives, endpoints, and outcomes
– Statistical Analysis, sample size considerations, data management
– Clinicaltrials.gov – outcome measure reporting

Audience: academic researchers, scientists, study coordinators, and students engaged in clinical research and/or clinical trials.

ACRP Contact Hours: 4.0 Contact Hours of clinical research education on the application for maintenance of ACRP’s ccrc®, ccra® or cpi®, certification designations will be available for attendees

If you have any other questions, please email Marie Rape at marie_rape@med.unc.edu.