- Clinical Trials
- Clinical Research Ethics
- Healthcare Ethics
- Science and Research
- Biostatistics
- Regulatory Compliance
- Good Clinical Practices (GCP)
- Clinical Research
- Informed Consent
Design and Conduct of Clinical Trials
Completed by Chad Maschinot
July 19, 2024
4 hours (approximately)
Chad Maschinot's account is verified. Coursera certifies their successful completion of Design and Conduct of Clinical Trials
What you will learn
Evaluate and select clinical trial designs
Implement bias control measures
Randomize participants into groups
Define clinical trial outcomes
Skills you will gain
