Clinical Research Associate (CRA) Beginners Online Course, September 5-20, 2022 –

Clinical Research Associate (CRA) Beginners Online Course, September 5-20, 2022 –

Clinical Research Associate (CRA) Beginners Online Course, September 5-20, 2022 –

DUBLIN–(BUSINESS WIRE)–The “CRA Beginners Online Course” training has been added to’s offering.

A CPD accredited intensive course which provides those starting or looking to improve their skills as a CRA with a comprehensive and valuable insight into the entry-level role of a Clinical Research Associate (CRA). How will i benefit from taking this course?

By the end of this course you will:

  • Identify suitable investigators to participate in a clinical trial
  • Perform pre-selection visits to assess the suitability of a site to conduct the trial
  • Understand what essential study documentations are required to start a trial
  • Conduct pre-trial activities including drug (IP) release procedures
  • Conduct an initiation visit
  • Monitor the conduct at the investigational site
  • Review source documentation and site file review
  • Perform site management activities
  • Conduct a close-out visit at the end of the study
  • Complete a clinical trial.

A clinical Research Associate (CRA) primarily manages the managerial aspects of a number of clinical trials, at every stage of the process. Who is the course designed for?

If you are a clinical trial administrator who has just been promoted to a CRA level I or have limited experience as a CRA, this modular training is specifically designed for you.

You may be a research nurse or a former data manager who has landed their first role as a CRA.

This is a good starter course that will equip you with the skills to conduct clinical trial initiation and/or monitoring and basic site management at the investigational site.

Key Topics Covered:

  • ICH- GCP
  • The primary duties of a CRA
  • The specific responsibilities in accordance with ICH-GCP, SOP and regulations:
  • Before the clinical phase of the trial commences
  • During the clinical conduct of the trial
  • After completion or termination of the trial
  • Essential documents- Preparation, collation and QC
  • Ethics and regulatory submissions and approvals of the clinical trial application
  • Study Start up activities- site identification and selection, QC for IP release
  • Site Activation- SIV, ISF review and Drug supply review
  • Monitoring and Site Management
  • Study site close out activities

For more information about this training visit


Laura Wood, Senior Press Manager

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