Clinical Research Associate Course
Master key CRA skills for healthcare: CAPA, informed consent, SDV, eligibility checks, SAE reporting, and IMP accountability. Learn practical monitoring strategies to protect patients, ensure GCP compliance, and strengthen your clinical research career.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
The Clinical Research Associate Course gives you practical, step-by-step training to monitor trials confidently and compliantly. Learn CAPA design, informed consent review, SDV and data integrity, eligibility checks, SAE detection and reporting, and IMP accountability. Build inspection-ready documentation skills and apply clear templates, SOP-based processes, and targeted monitoring strategies from day one.
Elevify advantages
Develop skills
- SAE safety oversight: detect, document, and escalate serious events fast.
- IMP accountability: reconcile drug logs, returns, storage, and temperature.
- Eligibility verification: confirm criteria and resolve source data conflicts.
- CAPA execution: design, document, and track corrective and preventive actions.
- Informed consent review: verify timing, signatures, and complete documentation.
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 workload.What our students say
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