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%

If you have a discount code this can be entered on the next page after clicking “Take This Course”

Take this Course

If you prefer to speak to someone call us on 0161 628 9626 and we'll be happy to help.

Sign up to our newsletter and receive 10% off your first course.