Clinical Research Associate (CRA) Training
This course equips you with essential skills for a Clinical Research Associate role, covering informed consent, ICH-GCP guidelines, oncology protocols, source data verification, corrective actions, and inspection readiness. Perfect for clinical professionals transitioning to impactful research positions in oncology and other studies.

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 workloadWhat our students say
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