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Clinical Research Coordinator Course

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

What will I learn?

The Clinical Research Coordinator Course provides practical, step-by-step training to handle source documentation, eCRFs, and data quality, while gaining expertise in informed consent and participant communication. You will learn ethics and regulatory strategies for a Phase II diabetes trial, safety reporting, confidentiality measures, and preparation for monitoring visits, enabling you to conduct compliant, inspection-ready studies with assurance.

Elevify advantages

Develop skills

  • Source and eCRF management: capture clean trial data quickly and ready for audits.
  • Informed consent expertise: conduct clear, ethical discussions with patients and maintain proper logs.
  • Safety and adverse event reporting: safeguard participants and adhere to strict regulatory deadlines.
  • IRB and regulatory files: compile complete binders and submissions for Phase II trials.
  • Monitoring visit preparation: successfully navigate sponsor visits and inspections with few issues.

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.
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 selected.
EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company where I work.
SilviaNurse
Very great course. Lots of valuable information.
WiltonCivil Firefighter

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