Clinical Trial Assistant (CTA) Course
Develop practical CTA expertise for clinical trials: gain command over GCP standards, adverse event reporting, informed consent processes, protocol adherence, CAPA development, and site interactions using tailored tools, checklists, and templates designed for Phase II hospital trials in asthma studies.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This Clinical Trial Assistant (CTA) Course delivers hands-on, step-by-step abilities to aid compliant asthma Phase II clinical studies. Master key GCP principles, protocol compliance, adverse event spotting, and precise source-to-eCRF matching. Acquire practical CAPA strategies, consent checking aids, logs, monitoring trackers, and messaging templates to boost data accuracy, cut down deviations, and maintain inspection preparedness.
Elevify advantages
Develop skills
- Master adverse event reporting: swiftly identify, record, and report safety issues.
- Achieve fluency in GCP and regulations: implement ICH guidelines, ethics, and AE protocols in routine trial tasks.
- Control informed consent: handle ICF updates, re-consenting, and maintain audit-compliant records.
- Build root cause analysis and CAPA expertise: investigate deviations and create strong corrective plans.
- Excel in CTA operations: assist with site monitoring, eCRF verification, and protocol enforcement.
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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