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Clinical Research Course

Clinical Research Course
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.
Workload: between 4 and 360 hours

What our students say

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The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Very great course. Lots of rich information.
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