Introduction to Clinical Research for Trial Coordinators: Part 1
Session Outline: A session that provides the background knowledge that will support staff to develop the skills required to attain the competency in the many and varied tasks associated with this pivotal role. This session focuses on
The session builds on the knowledge imparted during GCP training but also provides important foundational concepts that will help learners understand the contribution that well run trials make to science and society.
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:
• Understand the trial process, appreciate their value and be able to identify the attributes of a high-quality trial and the therapeutic goods development process
• Be familiar with the key players in research and their respective roles including the roles of ethics and governance and the key aspects of site-specific assessment
• Better understand the requirements of the NHMRC Safety Reporting Guidance
• Understand the requirements of the NHMRC Serious Breach Guidance
Certification: Attendees will receive a certificate of attendance following course completion.
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