As Clinical Research Professional, how to get the most out of your protocol for your day-to-day activities. This half-day course will focus on the content of a clinical trial protocol and how study design, statistics and risk management aspects as described in study protocol relate to your day-to-day monitoring activities, site management strategy, clinical data review, etc.
At the end, you will receive a certificate and the course hand-outs.
By the end of this TRIUM Training you should be able to:
- Explain the purpose and importance of a protocol in a clinical investigation
- List the minimal content requirements of a clinical trial protocol.
- Identify and explain important design and statistical concepts within your trial protocol
- List the requirements of risk management within trial protocols
Can perform the task and/or exhibit the knowledge at an essential or foundational level. May require some coaching or supervision.