Clinical Research Associate (CRA) Training
Gain essential skills as a Clinical Research Associate, covering informed consent processes, ICH-GCP guidelines, oncology trial protocols, source data verification, corrective actions, and inspection preparedness. Perfect for clinical professionals transitioning to impactful research monitoring roles in oncology and beyond.

4 to 360 hours of flexible workload
certificate valid in your country
What Will I Learn?
This focused Clinical Research Associate (CRA) Training course equips you with practical skills to monitor clinical trials effectively and in compliance. Key topics include ICH-GCP informed consent, regulatory documents, site file organisation, investigational product accountability, protocol deviations, source data verification, eCRF practices, serious adverse event management, corrective action plans, monitoring workflows, and inspection readiness for oncology and other studies.
Elevify Advantages
Develop Skills
- Master ICH-GCP and IRB requirements to conduct compliant, inspection-ready trials efficiently.
- Monitor oncology trials by verifying data accuracy, resolving queries, and ensuring patient safety.
- Manage protocols and investigational products, tracking deviations, dosing, and accountability.
- Oversee informed consent with version control, re-consent procedures, and IRB notifications.
- Develop CAPA plans and reports to document issues, identify trends, and enhance site performance.
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.What our students say
FAQs
Who is Elevify? How does it work?
Do the courses come with a certificate?
Are the courses free?
What is the course duration?
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 online course and how does it work?
PDF Course