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Discuss the roles and responsibilities of the key positions in the clinical trial process. Identify strategies for organizing clinical trials and site management to ensure a successful outcome of the trial. Gain a clear understanding of the role the regulatory environment plays in shaping the course of a clinical trial for both the sponsor and the investigative site.

Topics

  • The role of the investigative site
  • The role of the sponsor
  • Critical job functions along the delivery chain
  • The roles and responsibilities required for the planning and successful execution of a trial

Individual Course Registration

This course is part of the Diploma program and can also be taken as an individual course for non-credit/professional development.  How many courses can you take before you have to apply to the program? 

Diploma Program Progression

Successful completion of first term courses (Minimum 70% average with no single final grade below 65%) is required for progression to second term courses. Successful completion of first and second term courses is required for progression to practicum. 

Applies Towards the Following Certificates

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Type
Online
Dates
Sep 09, 2019 to Dec 06, 2019
Schedule
Total Hours
36.0
Format
Instructors
  • Michael Cornelius

What to Expect

This is an interactive course; you will engage online with your class and instructor through our online learning management system. Plan to log into your course regularly throughout the week.

You can expect approximately six hours of work per week for discussions, readings, assignments, exams/quizzes and other course requirements.

Completion Requirements

This is a graded course. Evaluation will be based on any combination of participation, exams/quizzes and assignments.

Textbook

Guide to Clinical Trials, Custom Course Package #M8277 (to be purchased using a voucher from the Western Bookstore)

Required