- Clinical Documentation
- Good Clinical Practices (GCP)
- Clinical Trials
- Record Keeping
- Regulatory Compliance
- Scientific Methods
- Clinical Research Ethics
- Institutional Review Board (IRB)
- Clinical Research
- Clinical Trial Management Systems
Clinical Trials Management and Advanced Operations
Completed by Vita Schothorst
October 10, 2024
4 hours (approximately)
Vita Schothorst'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
