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Clinical Research Training for Junior CRAs

Name: Clinical Research Training for Junior CRAs
Brand: ECCRT
Price: 1350 EUR
Rating: 5 (1 reviews)

Book a session

Date	Product	Location	Price
12/12/2024	Clinical Research Training for Junior CRAs	Amsterdam	EUR 1350	Book
26/03/2025	Clinical Research Training for Junior CRAs	Brussels	EUR 1350	Book
13/05/2025	Clinical Research Training for Junior CRAs	Online	EUR 1350	Book
02/07/2025	Clinical Research Training for Junior CRAs	Brussels	EUR 1350	Book
01/10/2025	Clinical Research Training for Junior CRAs	Brussels	EUR 1350	Book
If you would like to have this course as an in-house session click here

About this course

Reasons to attend

This Junior CRA training will train you in the basic, yet crucial areas within clinical monitoring. All typical tasks of a Clinical Research Associate (CRA) will become clear to you, from selecting the investigators until study site close-out, with a great focus on the “monitoring practice” and an introduction on the impact of digitalization.

What's included?

Documents and materials related to this course are included
Globally recognised certificates awarded after test completion

Course schedule

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

2-Day face-to-face: 09:00 - 17:00

4 webinar session

Course Description

Focussing on the different phases of the life cycle of a clinical trial, this Junior CRA training is specifically designed for people who have between zero to twelve months’ monitoring experience. The course covers all operational activities of monitoring. Dummy trial documents are used in the interactive workshops to share real-life operations. It is mandatory to have previously attended training on “Good Clinical Practice (GCP)”, as the aim of this course is to enable you as a CRA to implement the GCP requirements into your daily monitoring tasks. Become an expert in GCP with our classroom training or our eLearning course.

Programme highlight

Introduction to clinical research
Overview of the applicable legislation
The life cycle of a clinical trial
Monitoring activities from start to finish

Learning objectives

To outline the basis and phases of clinical research
Be able to recognise legislative requirements
Become familiar with the tasks expected from a CRA today
Be able to refer to essential trial documentation
How to deal with non-compliances

Who should attend

No previous knowledge of clinical research operations is required. However a Good-Clinical Practice Training is mandatory before attending this course.
A must for all inexperienced CRAs, experienced Clinical Trial Assistants or Clinical Trial Coordinator.
This course will also be beneficial for professionals in related areas such as clinical data processing, (bio-) statistics, regulatory affairs, project managers, etc.

Competencies

This course covers competencies that are part of the ECCRT Competency Framework

Scientific Concepts & Research Design (0)
Ethical & Participants Safety Considerations (5)
Investigational Product Development and Regulation (4)
Clinical Studies Operations (GCPs or ISO 14155) (8)
Study and Site Management (2)
Data Management and Informatics (4)
Leadership and Professionalism (0)
Communication (0)
Teamwork (0)
Business acumen (0)

Be aware that attending one of ECCRT public course does not guarantee that the competency is acquired but only guarantees that the related knowledge has been trained

Testimonials

Martha Chasapi

ECCRT provides very useful and high informative webinar training concerning junior CRAs. Very interesting things with details on the area of clinical research. In my opinion, ECCRT is the beginning of your career as CRA.
Anonymous

I feel like I have a good overall idea of the everyday work of a CRA. It was good to have some hands-on training for the monitoring activities as well. It was great to see how interactive the course was and how it was possible to ask questions and engage in conversation.
Adrian Manser

Swiss Pediatric Oncology Group
The course was very well organized. I liked the interactive style. I definitely refreshed my GCP knowledge and additionally, I learned a lot about the feasibility check of a study and the planning of pre-trial visits. I liked the short exercise at the end, where I together with an attendee performed possible monitoring with dummy material.
Sari Kassem

The course is very interactive and the instructor (Liesbeth) is a senior CRA, so her personal tips "experienced-based" were very useful. The course was tailored to be of great AID for both non-CRAs and provide some useful tips for those who are already CRAs.
Fien Hanssens

Harmony Clinical Research
The course was very interesting even if you have already experience as a CRA. Even if you don't have experience yet as a CRA, it is very understandable. Liesbeth did a great job!
Vlad Shtefaniuk

Uniqure Biopharma
Great course content and balanced duration
Eva Hansenne

BloomLife
The trainer was super great and gave lots of relevant examples from the field. It was a good mix of theory and practice. Moreover, we were a small group of trainees, so the training was interactive.
Daniela Budnila

Mirium Pharma
The trainer was very inclusive, treated each question seriously and engaged all participants. She also managed to stick to the agenda and time.