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 reporting to ensure high-quality trial execution.

from 4 to 360h flexible workload
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 execute Phase II protocols, manage site initiation and monitoring, ensure precise data and documentation, deal with SAEs and safety reporting, and implement risk-based oversight to keep trials compliant, efficient, and of high quality from start to close-out.
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 effectively: initiation, monitoring, risk-based oversight, and close-out.
- Manage trial data: eCRFs, queries, CAPA, and audit-ready records.
- Oversee safety: grade AEs, report SAEs/SUSARs, and assist 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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