Clinical Research Course
Gain mastery in oncology clinical research through hands-on training in ICH-GCP guidelines, ethical practices, protocol design, safety monitoring, and data management. Perfect for healthcare workers aiming for compliant trial execution and improved patient results in Kenyan and global settings.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This course delivers practical, step-by-step guidance on ICH-GCP, ethics, and regulations for oncology trials. Master informed consent management, Phase II protocol design and execution, site initiation and monitoring, precise data handling and documentation, SAE and safety reporting, plus risk-based oversight to keep trials compliant, efficient, and top-quality throughout.
Elevify advantages
Develop skills
- Design oncology Phase II trials with clear, feasible, GCP-compliant protocols.
- Apply ICH-GCP principles and ethics in managing consent, IRB submissions, and privacy.
- Efficiently run trial sites through initiation, monitoring, risk-based oversight, and close-out.
- Manage trial data using eCRFs, queries, CAPA, and maintain audit-ready documentation.
- Oversee safety by grading AEs, reporting SAEs/SUSARs, and supporting 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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