Clinical Research Associate Course
This course equips aspiring Clinical Research Associates with essential skills for effective trial monitoring, compliance, and documentation in clinical research settings.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
The Clinical Research Associate Course provides practical, step-by-step training to monitor trials confidently and in compliance. Learn CAPA design, informed consent review, SDV and data integrity, eligibility checks, SAE detection and reporting, and IMP accountability. Build skills for inspection-ready documentation 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 workloadWhat our students say
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