Monitoring Approved Research
This virtual workshop will consider local regulatory requirements and guidance related to monitoring of ethically approved research and clinical trials.
Facilitated by Dr Tim Dyke, Leading Well and Melanie Gentgall, CEO PRAXIS Australia
It will allow students to better understand the role, purpose and function of monitoring in clinical research, and the role and responsibility of the institution and HREC and other key stakeholders including researchers and research support staff.
Through group discussion and case scenarios, we will explore expectations and requirements so that all students have a clearer sense of the role of monitoring as a critical aspect of clinical research practice.
These sessions are applicable to :
- HREC Executive Officers
- Research Administrators
- Research Governance and Integrity Officers
- Research Managers/coordinators
$150 plus GST
- 22nd October, 10:00am – 12:00 midday AEST