Clinical Trial Assistant (CTA) Course
Acquire practical CTA competencies for clinical trials: excel in GCP principles, adverse event reporting, informed consent management, protocol compliance, CAPA development, and site liaison using tailored tools, checklists, and templates for Phase II hospital trials, ensuring data integrity and regulatory readiness.

4 to 360 hours flexible workload
valid certificate in your country
What will I learn?
The Clinical Trial Assistant (CTA) Course equips you with hands-on, sequential expertise to underpin compliant Phase II asthma studies. Master core GCP principles, protocol conformity, adverse event identification, and precise source-to-eCRF mapping. Obtain practical CAPA frameworks, consent validation aids, logs, monitoring trackers, and correspondence templates to enhance data accuracy, minimise deviations, and maintain inspection preparedness.
Elevify advantages
Develop skills
- Mastery in AE reporting: swiftly identify, record, and escalate safety incidents.
- Proficiency in GCP and regulations: implement ICH guidelines, ethics, and AE protocols in routine trial activities.
- Oversight of informed consent: handle ICF versions, re-consenting, and maintain audit-compliant records.
- Expertise in root cause analysis and CAPA: investigate deviations and develop robust corrective plans.
- Excellence in CTA operations: assist with monitoring, eCRF verification, and protocol adherence.
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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