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Clinical Research Coordinator Course

Clinical Research Coordinator Course
from 4 to 360h flexible workload
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. Learn ethics and regulatory strategies for a Phase II diabetes trial, safety reporting, confidentiality measures, and monitoring visit preparation so you can conduct compliant, inspection-ready studies with assurance.

Elevify advantages

Develop skills

  • Source & eCRF management: capture clean trial data quickly and ready for audits.
  • Informed consent mastery: conduct clear, ethical discussions with patients and maintain logs.
  • Safety & AE reporting: safeguard participants and adhere to strict regulatory deadlines.
  • IRB & regulatory files: assemble complete binders and submissions for Phase II trials.
  • Monitoring visit prep: 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

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