Certificate Program in Clinical Trials
NOTE: This certificate program may be completed entirely online!
OVERVIEW
Clinical Trials are a key tool in the evaluation of new strategies for prevention and treatment of disease. This certificate program focuses primarily on the design and analysis of randomized clinical trials for evaluation of licensed and non-licensed medical products and other health interventions, the regulatory framework for the conduct and evaluation of data from clinical trials, and ethical principles for the conduct of clinical trials.
EDUCATIONAL OBJECTIVES
After completing the certificate, students will be able to:
- Summarize the history of clinical trials and describe the role they play in evaluation of health interventions;
- Explain the key differences, advantages and disadvantages of experimental versus observational study designs;
- Develop a protocol, consent statement, monitoring plan and data collection plan for a clinical trial;
- Review and critique manuscripts presenting the results of clinical trials using CONSORT guidelines; and
- Explain the key ethical principles regarding the design, conduct and analysis of clinical trials
