Clinical Research Coordinator Course
This course equips aspiring Clinical Research Coordinators with essential skills for managing clinical trials, focusing on data handling, ethical practices, safety protocols, regulatory compliance, and preparation for audits and inspections in Phase II studies.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
The Clinical Research Coordinator Course provides practical, step-by-step training to handle source documentation, eCRFs, and data quality, while gaining expertise in informed consent and participant communication. Discover ethics and regulatory approaches for a Phase II diabetes trial, safety reporting, confidentiality measures, and preparation for monitoring visits to conduct compliant, inspection-ready studies with assurance.
Elevify advantages
Develop skills
- Source and eCRF management: capture clean trial data quickly and ready for audits.
- Informed consent expertise: conduct clear, ethical discussions with patients and maintain logs.
- Safety and AE reporting: safeguard participants and adhere to strict regulatory deadlines.
- IRB and regulatory files: assemble complete binders and submissions for Phase II trials.
- Monitoring visit preparation: succeed in sponsor visits and inspections with few issues.
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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