Clinical Research Professionals Online Training Courses

Course Information

 

 

This interactive an engaging online course has been designed to provide an in depth understanding of the roles and responsibilities of a CRA. On completion of this training, participants will be able to apply their knowledge and skills to become an effective CRA.

During this course you will learn how to:

 

 

  • Develop knowledge and understanding of what conducting a clinical trial entails,

  • Gain knowledge and understanding of the roles and responsibilities of sponsors, Ethics Committees/IRBs and monitors, before, during and after a clinical trial,

  • Learn why monitoring a clinical trial is essential to its efficacy and safety,

  • Consider the difference between centralised and on-site monitoring and when each approach is best used,

  • Establish an understanding of Risk-based monitoring and it’s practical application,

  • Investigate the Informed Consent process in detail and learn how to obtain informed consent,

  • Consider patient safety and how to record and report AE, SAE, ADR and SUSAR,

  • Define Essential Documents,

  • Determine what documentation is necessary before, during and after a clinical trial,

  • Develop an understanding of monitor responsibilities regarding Essential Documents,

  • Develop an understanding of monitor responsibilities regarding IP,

  • Learn how to maintain, store and verify essential documents including the use of EMR and eTMF,

  • Learn how to identify questionable data and deal with queries,

  • Develop an understanding of the purpose of audit and inspection and know how to prepare for them. 

Price: £349
All prices include VAT at 20%

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If you prefer to speak to someone call us on 0161 633 4594 and we'll be happy to help.

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