Clinical Research Course
This course offers hands-on training in clinical research for oncology trials, covering ICH-GCP compliance, ethical practices, protocol design, site management, data handling, and safety monitoring to ensure high-quality trial execution.

flexible workload from 4 to 360h
valid certificate in your country
What will I learn?
This Clinical Research Course provides practical, step-by-step training in ICH-GCP, ethics, and regulatory requirements for oncology trials. You will learn to handle informed consent, design and implement Phase II protocols, manage site initiation and monitoring, ensure precise data and records, deal with serious adverse events and safety reports, and use risk-based monitoring to keep trials compliant, efficient, and of high quality from beginning to end.
Elevify advantages
Develop skills
- Design oncology Phase II trials: create clear, workable, GCP-compliant protocols.
- Apply ICH-GCP and ethics: handle consent, IRB submissions, and privacy guidelines.
- Run sites efficiently: initiation, monitoring, risk-based oversight, and close-out.
- Manage trial data: eCRFs, queries, CAPA, and audit-ready documentation.
- Oversee safety: grade AEs, report SAEs/SUSARs, and support DSMB reviews.
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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