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. Topics to be discussed include: Federal Regulations Governing Human Subject Research, Tips for Protocol Adherence, Investigator Responsibilities, Informed Consent, Study Documentation, and Regulatory File Maintenance. This program is strongly encouraged for new investigators and coordinators as they start their clinical research careers as well as those with research experience.
Submit advance questions or comments to rcco@pitt.edu. Registration is required.
Wednesday, February 6 at 1:00 p.m. to 3:00 p.m.
RCCO Learning Resource Center, 3rd Floor, Room 305 3500 Fifth Avenue, Pittsburgh, PA 15213
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. Topics to be discussed include: Federal Regulations Governing Human Subject Research, Tips for Protocol Adherence, Investigator Responsibilities, Informed Consent, Study Documentation, and Regulatory File Maintenance. This program is strongly encouraged for new investigators and coordinators as they start their clinical research careers as well as those with research experience.
Submit advance questions or comments to rcco@pitt.edu. Registration is required.
Wednesday, February 6 at 1:00 p.m. to 3:00 p.m.
RCCO Learning Resource Center, 3rd Floor, Room 305 3500 Fifth Avenue, Pittsburgh, PA 15213