Clinical Research Coordinator Course
This course equips aspiring Clinical Research Coordinators with essential skills for managing Phase II clinical trials, focusing on data handling, ethics, safety, and regulatory compliance to ensure successful and compliant study execution.

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. Learn ethics and regulatory strategies for a Phase II diabetes trial, safety reporting, confidentiality measures, and monitoring visit preparation so you can conduct compliant, inspection-ready studies with assurance.
Elevify advantages
Develop skills
- Source & eCRF management: capture clean trial data quickly and ready for audits.
- Informed consent mastery: conduct clear, ethical discussions with patients and maintain logs.
- Safety & AE reporting: safeguard participants and adhere to strict regulatory deadlines.
- IRB & regulatory files: assemble complete binders and submissions for Phase II trials.
- Monitoring visit prep: succeed in sponsor visits and inspections with few issues.
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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