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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 Clinical Research Associate Training provides hands-on, step-by-step guidance to monitor clinical trials with confidence and in line with rules. You will learn to create CAPA plans, check informed consent forms, perform source data verification and maintain data accuracy, verify participant eligibility, spot and report serious adverse events, and track investigational medicinal products. Develop abilities to prepare documents ready for inspections and use straightforward templates, standard operating procedures, and focused monitoring methods right from the start.

Elevify advantages

Develop skills

  • SAE safety oversight: spot, record, and report serious events quickly.
  • IMP accountability: match drug records, returns, storage, and temperature conditions.
  • Eligibility verification: confirm participant criteria and fix source data issues.
  • CAPA execution: create, record, and follow up on corrective and preventive actions.
  • Informed consent review: check timing, signatures, and full 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

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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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