Good Research Practices

December 14, 2020 - 1:00pm


Overseeing a research study can be challenging, especially if you are new to the research environment. This workshop 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.

Register here if you are interested in attending the program. Submit advance questions or comments to

Kelly Dornin-Koss, Director, ECO-HSR
Melissa Miklos, Associate Diretor, HRPO
Maggie Soncini, ECO-HSR Coordinator

Dial-In Information

This is virtual event.  The link will be sent out prior to the event

Location and Address

This is a virtual event hosted by the Office of Research Protections, and the Human Research Protection Office.