Log in
Choose your language

Clinical Research Associate (CRA) Training

Clinical Research Associate (CRA) Training
from 4 to 360h flexible workload
valid certificate in your country

What will I learn?

Gain practical skills in this focused CRA Training to monitor clinical trials confidently and in compliance. Learn ICH-GCP informed consent, key regulatory documents, site file organisation, IP accountability, protocol deviations, SDV and eCRF practices, SAE management, CAPA development, monitoring workflows, and inspection preparation for quality oncology and non-oncology trials.

Elevify advantages

Develop skills

  • Master ICH-GCP and IRB essentials to run compliant, inspection-ready trials quickly.
  • Monitor oncology trials by verifying data, managing queries, and ensuring patient safety.
  • Control protocol and IP by tracking deviations, dosing windows, and drug accountability.
  • Lead informed consent processes with version control, re-consent steps, and IRB reporting.
  • Design CAPA and reports to document findings, trend issues, and improve site quality.

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

I was just promoted to Intelligence Advisor of the Prison System, and the course from Elevify was crucial for me to be chosen.
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

FAQs

Who is Elevify? How does it work?

Do the courses have certificates?

Are the courses free?

What is the course workload?

What are the courses like?

How do the courses work?

What is the duration of the courses?

What is the cost or price of the courses?

What is an EAD or online course and how does it work?

PDF Course