Clinical Research Associate (CRA) Training
Master the core skills of a Clinical Research Associate: informed consent, ICH-GCP, oncology protocols, SDV, CAPA, and inspection readiness. Ideal for clinical professionals moving into high‑impact clinical research roles.

from 4 to 360h flexible workload
certificate valid in your country
What will I learn?
This concise Clinical Research Associate (CRA) Training course builds practical skills to monitor trials confidently and compliantly. You will learn ICH-GCP–aligned informed consent requirements, essential regulatory documents, investigator site file structure, IP accountability, protocol deviations, SDV and eCRF best practices, SAE handling, CAPA design, monitoring visit workflows, and inspection readiness for high-quality oncology and non-oncology studies.
Elevify advantages
Develop skills
- Master ICH-GCP and IRB essentials: run compliant, inspection-ready trials fast.
- Monitor oncology trials: verify data, manage queries, and protect patient safety.
- Control protocol and IP: track deviations, dosing windows, and drug accountability.
- Lead informed consent: apply version control, re-consent steps, and IRB reporting.
- Design CAPA and reports: document findings, trend issues, and drive 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.What our students say
Your lessons are perfect. I purchased the one-year package and finally have the opportunity to follow various topics of my interest without needing to change platforms... I thank you for everything you do, I've already recommended you to other people...

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I like how the lessons are straight to the point and how I can change chapters and skip content I don't need.

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The platform is fast, simple to use. The diversity of content and complementary videos help a lot with learning.

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