- Regulatory Compliance
- Healthcare Ethics
- Informed Consent
- Good Clinical Practices (GCP)
- Clinical Research Ethics
- Clinical Trials
- Science and Research
- Clinical Research
- Biostatistics
Design and Conduct of Clinical Trials
Completed by Mary Ann Elemen Binuya
July 13, 2025
4 hours (approximately)
Mary Ann Elemen Binuya'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
