Clinical Trial Assistant (CTA) Course
Gain hands-on CTA skills for clinical trials in medicine. Master GCP principles, AE reporting, informed consent processes, protocol adherence, CAPA development, and site communications using practical tools, checklists, and templates designed for Phase II hospital trials. Strengthen data accuracy, cut down deviations, and prepare for inspections effectively.

from 4 to 360h flexible workload
certificate valid in your country
What will I learn?
This Clinical Trial Assistant (CTA) Course delivers practical skills for supporting compliant Phase II asthma studies. Master GCP basics, protocol compliance, adverse event spotting, and precise source-to-eCRF matching. Get CAPA plans, consent checks, logs, trackers, and comms templates to boost data quality, minimise deviations, and ensure inspection readiness.
Elevify advantages
Develop skills
- Master AE reporting: spot, record, and report safety issues fast.
- Gain GCP and regulatory know-how: use ICH, ethics, and AE guidelines daily.
- Handle informed consent: track ICF updates, re-consents, and audit files.
- Build root cause analysis and CAPA: fix deviations with solid plans.
- Excel in CTA tasks: aid monitoring, check eCRFs, ensure protocol follow-through.
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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