Clinical Research Course
This course equips healthcare professionals with essential skills in oncology clinical research, covering ICH-GCP compliance, ethical practices, protocol development for Phase II trials, vigilant safety monitoring, and robust data management. Participants will confidently conduct compliant trials, enhancing patient safety and research quality for better outcomes in clinical settings.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
Gain hands-on training in ICH-GCP guidelines, ethics, and regulations for oncology clinical trials. Master informed consent processes, Phase II protocol design and execution, site initiation and monitoring, precise data management and documentation, SAE handling and safety reporting, plus risk-based quality oversight to ensure trials remain compliant, efficient, and superior from initiation to closure.
Elevify advantages
Develop skills
- Design effective Phase II oncology trials with clear, practical, GCP-compliant protocols.
- Implement ICH-GCP standards and ethics, including consent management, IRB approvals, and data privacy.
- Efficiently manage trial sites through initiation, monitoring, risk-based approaches, and proper close-out.
- Handle trial data accurately using eCRFs, resolving queries, CAPA processes, and maintaining audit-ready records.
- Oversee participant safety by grading adverse events, reporting SAEs and SUSARs, and aiding DSMB evaluations.
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
FAQs
Who is Elevify? How does it work?
Do the courses have certificates?
Are the courses free?
What is the course workload?
What are the courses like?
How do the courses work?
What is the duration of the courses?
What is the cost or price of the courses?
What is an EAD or online course and how does it work?
PDF Course