Clinical Research Associate Course
Gain essential skills as a Clinical Research Associate in healthcare, covering CAPA management, informed consent processes, source data verification, eligibility assessments, SAE reporting, and IMP accountability. Acquire practical strategies for trial monitoring to safeguard participants, uphold Good Clinical Practice standards, and advance your career in clinical research with confidence and precision.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This course offers hands-on, step-by-step guidance for monitoring clinical trials effectively and in line with regulations. You will master CAPA planning, reviewing informed consent, source data verification, data integrity, patient eligibility screening, serious adverse event identification and reporting, plus investigational medicinal product tracking. Develop skills for creating inspection-ready records using standard templates, SOP-driven procedures, and focused monitoring techniques right away.
Elevify advantages
Develop skills
- SAE safety oversight: spot, record, and report serious events swiftly.
- IMP accountability: balance drug records, returns, storage, and temperature controls.
- Eligibility verification: validate criteria and fix source data issues.
- CAPA execution: plan, document, and monitor corrective and preventive actions.
- Informed consent review: check timing, signatures, and full 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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