
Dr. Marleen Verbeeck
Trainer
Marleen Verbeeck, is a trainer/coach and has been working at the European Centre for Clinical Research Training (ECCRT) since 2004.
She obtained her PhD in molecular biology at the University of Utrecht in 1990. After fundamental research positions at the universities of Utrecht, New York, Leuven and Maastricht, she changed her academic career in 1995. She gained solid grounding in clinical research, first as a clinical research associate, later as a medical writer combined with a position as trainer.
Marleen enjoys developing, lecturing, evaluating and developing comprehension tests of courses as well as boosting confidence and competence of clinical research professionals with different experience levels from the pharmaceutical, medical device industry and non-profit research organisations.
She has more than 15 years of educational expertise. She is author of scientific papers, clinical trial study protocols (phase I - IV) and clinical study reports. She has experience in medical areas such as : CNS, Gastroenterology, Gynaecology, Rheumathology, Cardiology, Oncology, Orthopaedics and Immonutherapy.
In addition, recently Marleen is also a regulatory consultant on European clinical trial legislation. Acquiring and conveying knowledge has always been her interest throughout her professional career.
LinkedIn Profile
Reasons to attend Clinical Research is one of the most regulated industries in the world. Not a sur...
Clinical Trial Regulations are known to be complex on the one hand, on the other hand, there is no w...
Reasons to attend Are you supporting a clinical team, responsible for filing and/or other administr...

Faced with a clinical study and uncertain how to deal with it? This course will take away your doubt...
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Reasons to attend This course is co-developed and given by the Belgian Competent Authorities. Europ...
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How to increase your odds of finding a job in Clinical Research? This STAR Programme will provide t...
The Medical Device world is fundamentally different from the Pharmaceutical environment: different p...
Do you need straightforward instructions on how to write an effective CAPA? Looking for a brief ex...
// MicroLearnings are bitesize, online learning activities (eLearning, instructional videos ...
// MicroLearnings are bitesize, online learning activities (eLearning, instructional videos ...
Reasons to attend If you are a clinical research professional, investigator, monitor or other staff...
Reasons to attend European legislation is often far away from daily life, yet in this interactive...
Reasons to attend The European Clinical Trial Regulation 536/2014, of April 2014, is to become the ...
Reasons to attend This interactive webinar was developed to help you understand the latest elements...
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