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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 regulations. 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 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

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EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Great course. A lot of valuable information.
WiltonCivil Firefighter

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