Clinical Research Associate (CRA) Training
Master core CRA skills like informed consent, ICH-GCP, oncology protocols, SDV, CAPA, an inspection readiness. Perfect fi clinical pros steppin into high-impact research roles, buildin confidence fi run compliant trials smooth.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
Dis concise CRA Training course build practical skills fi monitor trials confident an compliant. Yuh wi learn ICH-GCP align informed consent, key regulatory docs, investigator site file setup, IP accountability, protocol deviations, SDV an eCRF best practices, SAE handling, CAPA design, monitoring visit flows, an inspection readiness fi top-quality oncology an non-oncology studies.
Elevify advantages
Develop skills
- Master ICH-GCP an IRB essentials: run compliant, inspection-ready trials quick-quick.
- Monitor oncology trials: check data, handle queries, an protect patient safety proper.
- Control protocol an IP: track deviations, dosing windows, an drug accountability tight.
- Lead informed consent: use version control, re-consent steps, an IRB reporting right.
- Design CAPA an reports: document findings, spot trends, an boost site quality strong.
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 are saying
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