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, CAPA development, protocol deviation handling, and inspection readiness. Perfect for clinical professionals transitioning into impactful research roles in oncology and non-oncology studies.

4 to 360h flexible workload
certificate valid in your country
What will I learn?
Gain practical skills for confident, compliant trial monitoring in this CRA training. Cover ICH-GCP informed consent, key regulatory documents, site file organization, IP accountability, protocol deviations, SDV and eCRF practices, SAE management, CAPA creation, monitoring workflows, and inspection preparation for oncology and non-oncology trials.
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 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 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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