Roles and Responsibilties in Clinical Research

Roles and Responsibilities in Clinical Research

$199.00

Category:

Description

Roles and Responsibilities in Clinical Research is an online eLearning course that covers key roles and responsibilities of all major stakeholders involved in clinical research.

This course covers the duties of investigators, sponsors, vendors, IRBs, and clinical research staff, with a strong focus on ethics, compliance, and regulatory requirements. Learners will understand how these roles work together to protect study participants and ensure data quality. The course also highlights Good Clinical Practice (GCP) principles and applicable guidelines. It is designed to give professionals a clear and practical understanding of accountability throughout the clinical trial process.

The program is made up of 1 module, 4 topics and 5 Quizzes.

On completing your enrolment for the program you will instantly get access to our online learning portal.

Find more information about the field of Clinical Research – What is Clinical Research

Looking for a comprehensive program in Clinical Research? Explore our Diploma in Clinical Research program.

Key Features

  • Full access to e-Learning Portal containing Multimedia Tutorials and Quizzes.
  • Course Instructor support via Discussion Forums

Curriculum

  • Investigator Responsibilities
  • Sponsor-Vendor Responsibilities
  • IRB responsibilities
  • Role of Clinical Research Personnel

Sample Tutorial

Sample Tutorial – Investigator Responsibilities

Certification

At the end of the course, students will be awarded a certificate of completion.

Duration

The duration of this program is 2 months.

You will have access to the course on the learning portal, for the duration of the program.

Reviews

There are no reviews yet.

Be the first to review “Roles and Responsibilities in Clinical Research”

Your email address will not be published. Required fields are marked *

Related products