Overseeing a research study can be challenging, especially if you are new to the research environment. This webinar will provide an overview of the various components of Good Research Practices. This program is strongly encouraged for new investigators and coordinators as they start their clinical research careers, as well as those with research experience.

Topics to be discussed include: Federal Regulations Governing Human Subject Research, Protocol Development, Tips for Protocol Adherence, Investigator Responsibilities, Informed Consent and Waivers of Consent, Study Documentation, and Regulatory File Maintenance.

Presented by: 

Kelly Dornin-Koss, Director, ECS-HSR
Melissa Miklos, Associate Director, HRP
Maggie Soncini, Coordinator, ECS-HSR
 

(Zoom link provided upon registration.)