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Clinical Research Associate Course

Clinical Research Associate Course
4 to 360 hours of flexible workload
certificate valid 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. Learn CAPA design, informed consent review, SDV and data integrity, eligibility checks, SAE detection and reporting, and IMP accountability. Develop inspection-ready documentation skills and apply clear templates, SOP-based processes, and targeted monitoring strategies from day one.

Elevify Advantages

Develop Skills

  • SAE safety oversight: detect, document, and escalate serious events fast.
  • IMP accountability: reconcile drug logs, returns, storage, and temperature.
  • Eligibility verification: confirm criteria and resolve source data conflicts.
  • 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 Intelligence Advisor for the Prison System, 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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