Clinical Trial Assistant (CTA) Course
Gain practical CTA skills for clinical trials in medicine: master GCP principles, AE reporting, informed consent processes, protocol compliance, CAPA development, and site communication using tailored tools, checklists, and templates for Phase II hospital-based asthma studies. This course equips you with step-by-step guidance to ensure data quality, minimise deviations, and maintain inspection readiness in compliant trial support.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This Clinical Trial Assistant (CTA) Course delivers practical, step-by-step skills for supporting compliant Phase II asthma studies. Master GCP essentials, protocol adherence, AE detection, and precise source-to-eCRF reconciliation. Acquire ready-to-use CAPA plans, consent verification tools, logs, trackers, and communication templates to enhance data quality, cut down deviations, and remain inspection-ready throughout trial operations.
Elevify advantages
Develop skills
- Master AE reporting: detect, document, and escalate safety events swiftly.
- Achieve GCP and regulatory fluency: apply ICH, ethics, and AE rules daily.
- Control informed consent: manage ICF versions, re-consent, and audit files.
- Develop root cause and CAPA skills: analyse deviations and create action plans.
- Excel in CTA operations: support monitoring, eCRF checks, and protocol compliance.
Suggested summary
Before starting, you can change the chapters and the 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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