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

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This Clinical Trial Assistant (CTA) Training provides hands-on, step-by-step abilities to assist compliant asthma Phase II clinical studies. Master key GCP principles, protocol compliance, adverse event identification, and precise source-to-eCRF matching. Acquire practical CAPA strategies, consent checking resources, logs, monitoring trackers, and communication aids to boost data integrity, minimise deviations, and ensure inspection preparedness.
Elevify advantages
Develop skills
- Master adverse event reporting: swiftly identify, record, and report safety incidents.
- Achieve fluency in GCP and regulations: implement ICH guidelines, ethics, and AE protocols in routine operations.
- Control informed consent processes: handle ICF updates, re-consenting, and maintain audit-compliant records.
- Build root cause analysis and CAPA expertise: investigate deviations and create robust corrective plans.
- Excel in CTA operations: aid monitoring visits, verify eCRF data, and enforce protocol compliance.
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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