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Clinical Research Associate Course

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

What will I learn?

The Clinical Research Associate Course provides practical, step-by-step training to monitor trials confidently and in compliance with regulations. Learn CAPA design, informed consent review, source data verification and data integrity, eligibility checks, serious adverse event detection and reporting, and investigational medicinal product accountability. Develop skills for creating inspection-ready documentation and apply clear templates, SOP-based processes, and targeted monitoring strategies from the outset.

Elevify advantages

Develop skills

  • Serious adverse event safety oversight: detect, document, and escalate serious events swiftly.
  • Investigational medicinal product accountability: reconcile drug logs, returns, storage, and temperature conditions.
  • Eligibility verification: confirm criteria and resolve source data discrepancies.
  • CAPA execution: design, document, and track corrective and preventive actions.
  • Informed consent review: verify timing, signatures, and complete documentation.

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 Prison System Intelligence Advisor, and the course from Elevify was crucial for me to be the chosen one.
EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Great course. Lots of valuable information.
WiltonCivil Firefighter

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