Clinical Research Coordinator Course
Master the Clinical Research Coordinator role in healthcare. Learn informed consent, source documentation, AE/SAE reporting, data quality, ethics, and audit readiness so you can run safe, compliant, and inspection-ready clinical trials with confidence.

4 to 360 hours of flexible workload
valid certificate in your country
What Will I Learn?
The Clinical Research Coordinator Course gives you 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 Differentials
Develop Skills
- Source & eCRF management: capture clean trial data fast and audit-ready.
- Informed consent mastery: lead clear, ethical patient discussions and logs.
- Safety & AE reporting: protect participants and meet strict regulatory timelines.
- IRB & regulatory files: build complete binders and submissions for Phase II trials.
- Monitoring visit prep: pass sponsor visits and inspections with minimal findings.
Suggested Summary
Before starting, you can change the chapters and 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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