Clinical Research Course
This course equips learners with essential skills for conducting high-quality oncology clinical trials in compliance with ICH-GCP standards, covering protocol design, site management, data handling, and safety oversight.

4 to 360 hours 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. Learn to manage informed consent, design and conduct Phase II protocols, oversee site initiation and monitoring, ensure accurate data and documentation, handle SAEs and safety reporting, and apply risk-based oversight to keep trials 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 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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