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Clinical Research Course

Clinical Research Course
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 how 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 so trials remain 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, HREC 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.
Workload: between 4 and 360 hours

What our students say

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EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Great course. Lots of valuable information.
WiltonCivil Firefighter

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