Clinical Research Coordinator Course
Gain mastery as a Clinical Research Coordinator in healthcare settings. The course covers informed consent procedures, source documentation management, AE/SAE reporting, data quality assurance, ethical standards, and audit preparation. Equip yourself to manage safe, compliant, and inspection-ready clinical trials with full confidence and efficiency.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
This course offers hands-on, step-by-step guidance for handling source documents, eCRFs, and ensuring top-notch data quality. Gain expertise in informed consent processes, effective participant interactions, ethical practices, and regulatory strategies tailored for Phase II diabetes trials. Master safety reporting, confidentiality measures, and preparation for monitoring visits to conduct compliant, inspection-ready studies confidently.
Elevify advantages
Develop skills
- Source and eCRF management: Collect accurate trial data swiftly for audits.
- Informed consent expertise: Conduct ethical patient discussions and maintain records.
- Safety and AE reporting: Safeguard participants while adhering to regulatory deadlines.
- IRB and regulatory documentation: Prepare comprehensive files for Phase II trials.
- Monitoring visit preparation: Excel in sponsor audits with few discrepancies.
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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