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.


  • 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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