Brisbane –4th & 5th May 2016

Sydney – 21st & 22nd June 2016

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Introduction to Clinical Research Courses 2016 now enrolling for Sydney and Brisbane.

It can be overwhelming when you first start and this two-day course gives you both a broad overview of clinical research activities and regulations, as well as more in-depth information on key Study Coordinator responsibilities.  You will learn about the essential activities that contribute to a successful clinical trial including Good Clinical Practice, ethics, informed consent, clinical trial planning, managing essential documents, quality in clinical trials, data collection (particularly source documentation) and managing adverse event reporting.    You will understand what you have to do and how to interpret the particular requirements of Good Clinical Practice and other relevant regulations.  It is not enough just to be doing activities, it is critical to understand why you are doing them.  This helps you to develop processes and practical approaches that are efficient and ensure compliance with regulatory requirements.

Modules covered:

• The drug development process & overview of Australian clinical trial regulations
• GCP & GCP responsibilities
• Ethics in clinical trials
• Informed consent
• Quality in clinical trials
• Clinical trial management
• Data collection & trial management
• Safety assessments in clinical trials

Register Here