This 10-session course introduces the basics of clinical research design, including biostatistics, design of diagnostic and predictive test studies, and required/desired elements of clinical trial protocols. Participants will also gain an understanding of the regulatory aspects of clinical research conduct and oversight, Good Clinical Practice (GCP), and ethical dimensions of clinical research.
Open to faculty and staff. Classes held on Thursdays from 4:00 – 6:00 pm PT beginning January 14 through March 18, 2021.
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This course provides a step-by-step model for how to design and conduct clinical research. Session topics include the following:
- Getting Started: The Research Landscape
- Designing and Conducting RCTs
- Designing and Conducting Observational Studies
- Design and Analysis Tools for Diagnosis & Prediction
- Qualitative Research and Questionnaire Design
- Research Reproducibility, Data Management, and Collection
- Ethics and Clinical Research
- Developing a Clinical Protocol
- Implementing a Clinical Protocol
- What’s Next
Sessions taught by Stanford faculty and staff who are experts in the field of clinical research.
Questions? Contact Course Coordinator, Jessica Meyer MBA, at [email protected]
- Study Design
- Ethics
- Data Reproducibility
- Education and Training
- Clinical Research
- CTSA Program
Date
Thursday, January 14, 2021 – 07:00 pm EST – Thursday, March 18, 2021 – 07:00 pm EDT
Activity Type
Conference
Organization
Stanford University
Location Type
Online