Clinical Research Training for Clinical Trial Assistants (CTAs)

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Beschrijving

Clinical Research Training for Clinical Trial Assistants (CTAs)

Course Description

Personnel entering clinical research for the first time and having less than one year’s experience have a great need for information and assistance in order to perform this function.

This two-day course will guide you through your responsibilities (GCP and others) and shows you how to document, record, file and archive trial material. It covers the basics and regulatory principles that underpin clinical research and also provides a practical coverage of the day to day functions. Theory and interactive exercise make this training the ideal foundation for a career as a CTA.

Learning objectives

  • To introduce t…

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Nog niet gevonden wat je zocht? Bekijk deze onderwerpen: Inbraakbeveiliging, Voedselveiligheid, Informatiebeveiliging, Beveiliging en ICT Management & Strategie.

Clinical Research Training for Clinical Trial Assistants (CTAs)

Course Description

Personnel entering clinical research for the first time and having less than one year’s experience have a great need for information and assistance in order to perform this function.

This two-day course will guide you through your responsibilities (GCP and others) and shows you how to document, record, file and archive trial material. It covers the basics and regulatory principles that underpin clinical research and also provides a practical coverage of the day to day functions. Theory and interactive exercise make this training the ideal foundation for a career as a CTA.

Learning objectives

  • To introduce the new Clinical Trial Assistants to drug development
  • To clarify the difference between medical care and clinical trials
  • To be familiar with the new CTA with ICH-Good Clinical Practice (GCP) rules
  • To present the processes of a clinical trial from beginning to end
  • To explain the why, when and how of essential study documents

Programme highlights

  • ICH-GCP as the basis of Clinical Research
  • ICH-GCP essential documents – sponsor and study centre requirements
  • Trial Master Files and Investigator Files


Workshops
• Essential study documents: cases
• Management of files
• Quiz on ICH-GCP and essential study documents

• Comprehension Test at the end of the course (included in the price)

Who should attend

CTAs who are relatively new to the job This course will also be beneficial to people working in other areas

*Due to unforeseen circumstances, the programme may change and the ECCRT reserves the right to alter the venue or cancel the event.

Trainer: Marleen Verbeeck, PhD

Language: English

Important: In case you have more than 5 interested participants you can save about 50% of your costs by inviting the trainer over for a tailored on-site training

What did our participants think ? Kyriaki Tsigkari, Medical Affairs Specialist - Clinical Research Training for Clinical Trial Administrators participant 2010 - Shire Hellas Greece

"I would like to thank you for the very helpful and informative CTA training. The content and the organisation were of high quality and I am happy I had the opportunity to participate. Also, I am really grateful for your assistance in getting to the training centre this morning! It was very kind of you! I hope that we will have the chance to meet and work together again in the future."

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