Clinical Protocol Development Workshop

The goal of this workshop is to provide researchers with knowledge, tools and resources to aid in the development of a scientific protocol for a clinical research study. This 2.5 hour workshop will focus on the following key points:

• Who needs a clinical protocol and why it is important
• Types of clinical protocols
• Protocol problems spots and ways to improve protocols
• Resources and tools available at UNC to support clinical protocol development

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

In-person attendance is strongly encouraged as this workshop will include many opportunities to ask questions of and interact with the speakers; however, for those who cannot attend in person due to travel concerns, we will be recording the workshop and will have a remote attendance link. Please contact Amanda Wood at amanda_wood@med.unc.edu for the remote attendance link.

ACRP Contact Hours: 2.5 Contact Hours of clinical research education on application for maintenance of ACRP's ccrc®, ccra® or cpi®, certification designations will be available for attendees