CTMG6003 - Organization and Monitoring of Clinical Trials I

This course is part of our Post-Degree Diploma in Clinical Trials Management.

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

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.