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, protocol and IP accountability, SDV practices, CAPA development, and inspection readiness. Perfect for clinical professionals transitioning into impactful research roles in oncology and non-oncology studies.

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. Covers ICH-GCP informed consent, key regulatory documents, site file organisation, IP accountability, protocol deviations, SDV and eCRF best practices, SAE management, CAPA creation, monitoring workflows, and inspection preparation for oncology and non-oncology studies.
Elevify advantages
Develop skills
- Master ICH-GCP and IRB essentials to run compliant, inspection-ready trials efficiently.
- 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, identify trends, 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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