What You Will Learn!
- This program will teach you about Clinical Research, Phases in Clinical Research, ICH-GCP guidelines, Protocol, Roles and Responsibilities of Investigator, Monitor or Coordinator etc.
- You can kick start your career as CRC or Monitor, along with some experience in Clinical Research Industry.
Description
This program will help participants to learn Clinical Trial Process/ Clinical Operations. Program starts with an Introduction followed by Phases in Clinical Trial Process, ICH- GCP guidelines, Stakeholders in Clinical Research and their responsibilities in Clinical Trial. Program gives and overview rather an in-depth details. If you are looking to get first hand information about clinical research, this program can be the right fit.
Who Should Attend!
- Life Science, Pharma, Nursing, Medical and Clinical Research Professionals
Tags
- Clinical Research
- Good Clinical Practice
Subscribers
166
Lectures
7
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