Clinical Research Associate (CRA) Training
This course equips aspiring Clinical Research Associates with essential skills in ICH-GCP compliance, informed consent management, oncology trial monitoring, source data verification, corrective action plans, and inspection readiness. Perfect for clinical professionals transitioning into impactful research roles, it covers regulatory documents, site files, IP accountability, protocol deviations, SAE handling, and monitoring workflows for high-quality studies in oncology and beyond.

4 to 360 hours flexible workload
valid certificate in your country
What will I learn?
Gain practical skills for confident, compliant trial monitoring in this CRA training. Learn ICH-GCP informed consent, key regulatory documents, site file setup, IP tracking, protocol deviations, SDV and eCRF practices, SAE management, CAPA creation, visit workflows, and inspection prep for oncology and other studies.
Elevify advantages
Develop skills
- Master ICH-GCP and IRB essentials to run compliant, inspection-ready trials.
- Monitor oncology trials by verifying data, managing queries, and ensuring patient safety.
- Control protocols and IP through 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 the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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