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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 records, deal with serious adverse events and safety reports, and use risk-based approaches to keep trials compliant, efficient, and of high quality from beginning to end.

Elevify advantages

Develop skills

  • Design oncology Phase II trials: create clear, workable protocols that follow GCP.
  • Apply ICH-GCP and ethics: handle consent, IRB approvals, and privacy guidelines.
  • Run sites well: start up, monitor, use risk-based checks, and close out properly.
  • Manage trial data: use eCRFs, fix queries, apply CAPA, and prepare documents for audits.
  • Oversee safety: assess AEs, report SAEs/SUSARs, and assist 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 where I work.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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