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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 manage informed consent, design and implement Phase II protocols, oversee site initiation and monitoring, ensure accurate data and documentation, handle serious adverse events and safety reporting, and apply risk-based oversight to keep trials 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, 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 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 are saying

I was just promoted to Intelligence Advisor for the Prison System, and the course from Elevify was crucial for me to be the chosen one.
EmersonPolice Investigator
The course was essential to meet my boss's and the company's expectations.
SilviaNurse
Really great course. Lots of valuable information.
WiltonCivil Firefighter

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