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Clinical Research Coordinator Course

Clinical Research Coordinator Course
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 & 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 the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.
Workload: between 4 and 360 hours

What our students say

I was just promoted to Intelligence Advisor for the Prison System, and the course from Elevify was crucial for me to be chosen.
EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Great course. Lots of valuable information.
WiltonCivil Firefighter

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