Clinical Research Course
Master clinical research in oncology with practical training in ICH-GCP, ethics, protocol design, safety monitoring, and data quality. Ideal for healthcare professionals seeking confident, compliant trial conduct and stronger patient outcomes.

flexible workload from 4 to 360h
valid certificate in your country
What will I learn?
This Clinical Research Course gives you practical, step-by-step training in ICH-GCP, ethics, and regulatory expectations for oncology trials. Learn how to manage informed consent, design and run Phase II protocols, oversee site initiation and monitoring, ensure accurate data and documentation, handle SAEs and safety reporting, and apply risk-based oversight so trials stay compliant, efficient, and high quality from start to close-out.
Elevify advantages
Develop skills
- Design oncology Phase II trials: build clear, feasible, GCP-compliant protocols.
- Apply ICH-GCP and ethics: manage consent, IRB submissions, and privacy rules.
- 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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