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Clinical Research Associate Course

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

What will I learn?

This course offers hands-on, step-by-step guidance for monitoring clinical trials effectively and in line with regulations. You will master CAPA planning, reviewing informed consent, source data verification, data integrity, patient eligibility screening, serious adverse event identification and reporting, plus investigational medicinal product tracking. Develop skills for creating inspection-ready records using standard templates, SOP-driven procedures, and focused monitoring techniques right away.

Elevify advantages

Develop skills

  • SAE safety oversight: spot, record, and report serious events swiftly.
  • IMP accountability: balance drug records, returns, storage, and temperature controls.
  • Eligibility verification: validate criteria and fix source data issues.
  • CAPA execution: plan, document, and monitor corrective and preventive actions.
  • Informed consent review: check timing, signatures, and full documentation.

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 chosen.
EmersonPolice Investigator
The course was essential to meet my boss's and the company's expectations.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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