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

4 to 360 hours of flexible workload
certificate valid 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. You will learn ethics and regulatory strategies for a Phase II diabetes trial, safety reporting, confidentiality measures, and preparation for monitoring visits, enabling you to conduct compliant, inspection-ready studies confidently.
Elevify Advantages
Develop Skills
- Source and eCRF management: capture clean trial data quickly and in audit-ready form.
- Informed consent mastery: conduct clear, ethical discussions with patients and maintain proper logs.
- Safety and AE reporting: safeguard participants and adhere to stringent regulatory deadlines.
- IRB and regulatory files: compile comprehensive binders and submissions for Phase II trials.
- Monitoring visit preparation: successfully navigate 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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