Clinical Research Coordinator Course
This course equips aspiring Clinical Research Coordinators with essential skills to manage clinical trials effectively, ensuring compliance, data integrity, and participant safety in Phase II studies.

4 to 360 hours flexible workload
valid certificate in your country
What will I learn?
The Clinical Research Coordinator Course provides practical, step-by-step training to manage source documentation, eCRFs, and data quality, while mastering informed consent and participant communication. Learn ethics and regulatory strategy for a Phase II diabetes trial, safety reporting, confidentiality controls, and monitoring visit readiness so you can run compliant, inspection-ready studies with confidence.
Elevify advantages
Develop skills
- Source and eCRF management: capture clean trial data quickly and audit-ready.
- Informed consent mastery: lead clear, ethical patient discussions and logs.
- Safety and AE reporting: protect participants and meet strict regulatory timelines.
- IRB and regulatory files: build complete binders and submissions for Phase II trials.
- Monitoring visit preparation: pass sponsor visits and inspections with minimal findings.
Suggested summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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