training

Introduction to and Orienting Your Career in Clinical Research

translational research
live training

Introduction to and Orienting Your Career in Clinical Research

Target Audience:
VIB PhD Student
VIB Postdoc
VIB Staff Scientist
Location:

Ghent - VIB/UGent FSVM II

Duration:

7 September 2023

General context

The first part of this course will focus on the elementary aspects of clinical research. Through an interactive step-by-step approach, we will introduce you to the world of medicine before they are available on the market. This course is designed to allow you to get familiar with the basic aspects of pre-clinical and clinical studies, the rules and regulations to follow, the ethical considerations and follow-up of trial participants, the involved logistics and resources.

A second topic will be on orienting your career in clinical research. This part of the training will provide you with an overview of the job possibilities that are out there in the clinical development area and in clinical research. 

Objectives

After this training, you will:

  • understand all steps of how a pharmaceutical product gets to the market.
  • know the difference between pre-clinical and clinical research
  • understand why clinical research is performed
  • identify how clinical researchers are set-up and the logistic it involves.
  • know what the different positions in clinical research are
  • understand the Clinical Research Competency Framework
  • see what the best steps are to find a job in Clinical Research

 

Approach

ECCRT aims for the best return on investment for the participant. Our goal is for trainees to leave the course with the capacity to use the information provided in the most practical way. Our expert trainers always encourage interactivity in the group. ECCRT supports the statement: “You tell me, and I forget. You teach me, and I remember. You involve me, and I learn”.

Event intended for

PhD students, postdocs and staff scientists working at VIB who have an interest in understanding the basics of the current regulatory requirements for clinical trials. We will also address career opportunities in clinical research.

Extra information
  • This training is free for VIB participants.
  • Note that upon no show without valid justification a fee of € 100 will be charged and you will be blacklisted for the VIB training program for 1 year. Click here for more information
Testimonials
testimonials

I was overall very pleased with this training, it was very interesting and the trainer explained everything in a very engaging, enthusiastic manner.

Participant edition 2022

The training gave us good insights in future job opportunities in the field, where you can decide for yourself if you are interested in them or not. Handy tips and tricks were given for job applications. There was also a good overview of what clinical research entails.

Participant edition 2021

Trainers

Benedikt Van Nieuwenhove

Prof. Dr. Benedikt Van Nieuwenhove obtained his degree in Pharmaceutical sciences from the University of Gent, Belgium in 1991. Between 1991 and 1997 he worked as a quality assurance manager at a laboratory for medical biochemistry & clinical analysis in Gent.  In 1997 he finished his Ph.D. in Pharmaceutical Sciences at the University of Gent in Belgium. 

Since then till 2014 he had been working for Harrison Clinical Research. He started his career as clinical operations manager and general manager of the Benelux operations.

In 2000, he founded their own training Academy, the "European Centre for Clinical Research Training” (ECCRT) and in 2007 he became a member of the Board.

From 2008-2011 he acted as the Vice President Global Operations of the Harrison Clinical Research group. In January 2011, he was elected Chief Executive Officer of Harrison Clinical Research. In that position he was involved in the merge with Synteract to form SynteractHCR. He has been instrumental in integrating the two organisations during 2013 and 2014.

Since its creation in 2000, Benedikt has been the Managing Director of ECCRT.

Having been in the field of Clinical Research for about three decades he has amassed a wealth of knowledge and skills within this field. Over the years he has supported the Pharma Industry as well as other players in the healthcare sector by providing them with the skill sets to deal with the challenges in their job and to make them efficient players in study success.

Since 2016 he is lecturing “Management of Clinical Research” at the Faculty of Pharmaceutical Sciences, University Ghent.

Liesbeth Lemmens

Liesbeth Lemmens holds a bachelor’s degree in Nursing and obtained a master’s degree in Medico-Social Sciences at the Catholic University of Leuven. Her professional experience is a mix of 20 years working in clinical research, as a clinical trial coordinator, project manager and CRA (oncology, cardiology and IBD). In 2010, she started to work as an independent consultant for health care providers. Mrs. Lemmens is also key opinion leader in educating health care providers, clinical research associates, clinical trial assistants and (data) managers on different topics, such as: − ICH-GCP in daily practice − Audit and inspection readiness − Train the trainer − Time management in clinical research − Developments and therapies in oncology. She teaches in terms of the most-up-to-date knowledge delivered in an accessible and informative fashion, with constant updating of training materials. As a facilitator and moderator, she uses a wide range of skills and tools, from problem solving and decision making, to team and time management, coaching and communications.

Program

Introduction to Clinical Research

-

Welcome & introduction

Clinical Research

  • How are new medicinal products developed
  • What is Clinical Research?
  • What are the different types of clinical trials o Why are clinical trials regulated?
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Coffee break

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  • What are the clinical research principles?
  • What activities are involved in clinical trials?
  • What are the logistics behind clinical trials?
  • Who is involved in clinical research?
-

Conclusions and Q&A

-

Lunch

Orienting your career in clinical research

-

Welcome & introduction

-

The clinical competency framework

-

Coffee break

-

Mapping of profiles versus positions

-

Recommendations for finding a job in clinical research

-

Conclusions and Q&A

Practical info

Location & Venue

07 September 2023

Ghent - VIB/UGent FSVM II

Technologiepark 75
9052 Zwijnaarde
Belgium

Public transport

07 September 2023

Ghent - VIB/UGent FSVM II
Public transport

From Ghent Sint-Pieters station, you can take bus 49, 50 or 70 to Technologiepark. Please check Routeplanner De Lijn for schedules.

Route description

07 September 2023

Ghent - VIB/UGent FSVM II
Parking

Route description

There is only one entrance to Technologiepark. At the entrance, please take a ticket and have it validated at the reception desk of the FSVM building. Parking will only be allowed in regular parking spots (for instance in front of the building) and in the new parking tower. Parking alongside the roads or in other places where there is no regular parking is prohibited and after initial warnings, fines will be issued (€ 50).

Venue contact

07 September 2023

Ghent - VIB/UGent FSVM II
Extra information

Room L4