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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?

The Clinical Research Associate Course provides practical, step-by-step training to monitor trials confidently and in compliance with standards. You will learn to design CAPA, review informed consent, perform SDV and ensure data integrity, check eligibility, detect and report SAEs, and manage IMP accountability. Develop skills for creating inspection-ready documentation using clear templates, SOP-based processes, and targeted monitoring strategies right from the start.

Elevify advantages

Develop skills

  • SAE safety oversight: detect, document, and escalate serious events quickly.
  • IMP accountability: reconcile drug logs, returns, storage, and temperature conditions.
  • 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 of 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 where I work.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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