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. The first day of the series will provide an introduction and focus on the following key points:<\/p>\n
– Who needs a clinical protocol and why it is important
\n– Types of clinical protocols, and content expectations for sections of the protocol
\n– Introduction to clincaltrials.gov registration
\n– UNC Scientific Review processes
\n– Protocol problems spots and ways to improve protocols
\n– Resources and tools available at UNC to support clinical protocol development<\/p>\n
On the second day of the series we will take a “deeper dive” into clinical study design,
\nstatistics, and their impact on clinicaltrials.gov reporting:
\n– Clinical Protocol Study Design – aims, objectives, endpoints, and outcomes
\n– Statistical Analysis, sample size considerations, data management
\n– Clinicaltrials.gov – outcome measure reporting<\/p>\n
Audience: academic researchers, scientists, study coordinators and students engaged in clinical research and\/or clinical trials.<\/p>\n
ACRP Contact Hours: 4.0 Contact Hours of clinical research education on application for maintenance of ACRP’s ccrc\u00ae, ccra\u00ae or cpi\u00ae, certification designations will be available for attendees.<\/p>\n","protected":false},"excerpt":{"rendered":"