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Clinical Research Course

Clinical Research Course
4 to 360 hours of flexible workload
valid certificate in your country

What Will I Learn?

This Clinical Research Course gives you practical, step-by-step training in ICH-GCP, ethics, and regulatory expectations for oncology trials. Learn how to manage informed consent, design and run 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 stay compliant, efficient, and high quality from start to close-out.

Elevify Differentials

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 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. A lot of valuable information.
WiltonCivil Firefighter

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