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Introduction to Clinical Research for Trial Coordinators: Part 2

Session Outline: A session that provides the background knowledge that will support staff to develop the skills required to attain the competency in some key tasks associated with this pivotal role. The session builds on the knowledge imparted during GCP training, drilling down on key activities, including informed consent, trial recruitment and trial documentation.

Price: 2-hour session: $1000 + GST for up to 15 attendees  

Mode of delivery: Live, interactive Zoom session    

Duration: 2 hours

Learning Objectives: Attendees will be able to:         
  • Better understand the requirements for informed consent
  • Identify common barriers to recruitment to research and mechanisms to help address slow recruitment
  • Appreciate the requirements for information governance (privacy and confidentiality)
  • Confidently apply the requirements of the NHMRC Safety Reporting Guidance
  • Better understand the requirements for generating, managing, and archiving trial documentation    


Certification: Attendees will receive a certificate of attendance following course completion.
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