Log in
Choose your language

Clinical Research Coordinator Course

Clinical Research Coordinator Course
from 4 to 360h flexible workload
certificate valid 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 to conduct compliant, inspection-ready studies confidently.

Elevify advantages

Develop skills

  • Source and eCRF management: capture clean trial data quickly and ready for audits.
  • Informed consent mastery: conduct clear, ethical discussions with patients and maintain logs.
  • Safety and AE reporting: safeguard participants and adhere to strict regulatory deadlines.
  • IRB and regulatory files: prepare complete binders and submissions for Phase II trials.
  • Monitoring visit preparation: succeed in 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 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 where I work.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

FAQs

Who is Elevify? How does it work?

Do the courses have certificates?

Are the courses free?

What is the course workload?

What are the courses like?

How do the courses work?

What is the duration of the courses?

What is the cost or price of the courses?

What is an EAD or online course and how does it work?

PDF Course