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Clinical Research Coordinator Course

Clinical Research Coordinator Course
flexible workload of 4 to 360h
valid certificate in your country

What will I learn?

This course offers hands-on, step-by-step guidance for handling source documents, eCRFs, and ensuring top-notch data quality. Gain expertise in informed consent processes, effective participant interactions, ethical practices, and regulatory strategies tailored for Phase II diabetes trials. Master safety reporting, confidentiality measures, and preparation for monitoring visits to conduct compliant, inspection-ready studies confidently.

Elevify advantages

Develop skills

  • Source and eCRF management: Collect accurate trial data swiftly for audits.
  • Informed consent expertise: Conduct ethical patient discussions and maintain records.
  • Safety and AE reporting: Safeguard participants while adhering to regulatory deadlines.
  • IRB and regulatory documentation: Prepare comprehensive files for Phase II trials.
  • Monitoring visit preparation: Excel in sponsor audits with few discrepancies.

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 of 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
Very great course. Lots of rich information.
WiltonCivil Firefighter

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