This course presents history, principles, best practices, and benefit/risk analysis regarding the rights and welfare of human participants in research. Both the ethics regarding human subjects’ research and the regulations for such research will be presented. Ethical case scenarios are incorporated into the training so the participant can apply various concepts. The seminar also looks at future initiatives for protection of human subjects.
- Examine the history of research ethics
- Apply principles of clinical research ethics and understanding why they are necessary
- Recognize research practices for protection of trial participants: team roles and responsibilities
- Identify susceptible populations, and specific safeguards for their protection
- Examine the effectiveness of current best practices
- Investigators
- IRB Members
- Clinical Research Coordinators
- Site Research Managers
- Clinical Research Monitors
- Sponsor Project Managers
Sandra “SAM” Sather, MS, BSN, CCRA, CCRC
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2 hours; 12:30 - 2:30 p.m. Eastern
May 24, 2010
Hold this course at your company!
For more information, contact Naila Ganatra at (215) 413-2471