- Clinical Research Ethics
- Institutional Review Board (IRB)
- Clinical Trial Management Systems
- Regulatory Compliance
- Clinical Research
- Clinical Documentation
- Good Clinical Practices (GCP)
- Clinical Trials
- Record Keeping
- Scientific Methods
Clinical Trials Management and Advanced Operations
Completed by K ACHYUTH
March 12, 2024
4 hours (approximately)
K ACHYUTH's account is verified. Coursera certifies their successful completion of Clinical Trials Management and Advanced Operations
What you will learn
Detect and respond to protocol events
Recognize and respond to misconduct
Safeguard participant safety and trial integrity
Develop and maintain study documents
Skills you will gain
