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Clinical Research Course

Clinical Research Course
from 4 to 360h 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. You will learn to handle informed consent, design and implement Phase II protocols, manage site initiation and monitoring, ensure precise data and documentation, deal with SAEs and safety reporting, and use risk-based oversight to keep trials compliant, efficient, and high quality from beginning to end.

Elevify advantages

Develop skills

  • Design oncology Phase II trials: create clear, workable, GCP-compliant protocols.
  • Apply ICH-GCP and ethics: handle consent, IRB submissions, and privacy guidelines.
  • 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 where I work.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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