Clinical Research Training for Senior CRAs - Blended - ECCRT
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Clinical Research Training for Senior CRAs – Blended

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14/10/2024Clinical Research Training for Senior CRAsBrusselsEUR 1325.00Book
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Senior Clinical Research Training Course ECCRT

About this course

Reasons to attend

Do you want to refresh and improve your CRA skills?  Do you need some inspiration to boost your clinical trial monitoring techniques and approach?

This CRA Training provides for experienced monitors the knowledge and advanced skills to deal with more complex clinical trials and site management issues. This training, supported by eLearning, provides the best outcome allowing you to learn at your own pace. Increase your odds of becoming a senior CRA with this training.

What's included?

  • Documents and materials related to this course are included
  • Globally recognised certificates awarded after test completion
  • This course has been granted PharmaTrain Recognition

Course schedule

We provide this course in two distinct formats: Classroom OR Online

This course is a blended learning course, which means it is broken into two parts. The eLearning session must be attended before the face to face training as its content fits to the practical approach during face-to-face training.

Classroom with eLearning:

  1. eLearning: 6 hours
  2. 1-Day face-to-face: 09:00 - 17:00

Webinars with eLearning:

  1. eLearning: 6 hours
  2. 2 webinar sessions

Course Description

Through an interactive approach, in this blended learning course, you receive a concise update of the current European clinical trial legislation and you will learn more about clinical trials in developing countries. The critical milestones of clinical trials, contingency plans, dealing with non-compliances, risk-based monitoring, your relationship with the investigator, and coaching junior CRAs are the main topics of this course.

The live session (F2F or webinar) will implement the eLearning material in practice: how to upgrade monitoring methods and skills, how to select the right investigators, how to boost subject recruitment, how to detect and correct informed consent issues, how to solve site management matters and how to deal with non-compliance. You gain insights in developing monitoring plans, tracking tools, accurate monitoring visit reporting, and corrective and preventive actions. You will be reviewing cases from real-life situations during workshops. Lively discussion and action planning involving real-life cases in the live session is one of the main learning areas.

Here you will benefit not only from the trainers but also learn from each other’s experiences.

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