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
This 4 Day STAR Programme is intended for CRAs wishing to boost their career. As a more experie...
Clinical Research is one of the most regulated industries in the world. Not a surprise, as we are de...
Are you supporting a clinical team, responsible for filing and/or other administrative tasks concer...
Are you supporting a clinical team, responsible for filing and/or other administrative tasks? This 2...
Do you want to refresh and improve your CRA skills? Do you need some inspiration to boost your cli...
Faced with a clinical study and uncertain how to deal with it? This course will take away your doubt...
You want to see the difference between the legislations in Europe and the United States? Discover th...
This programme aims to help you obtaining the ACRP certification. This training path, combining face...
This course is co-developed and given by the Belgian Competent Authorities. European legislation is ...
Did you know that your clinical investigations need to comply with the Good Clinical Practice (G...
Did you know that your clinical investigations need to comply with the Good Clinical Practice (GCP...
This course is for all those who need to grasp the essence, but not all the details of the Good Clin...
You need to update and refresh your knowledge on ICH-GCP , including the ICH-GCP E6 (R2) Addendum 20...
You need to update and refresh your knowledge on ICH-GCP, including the ICH-GCP E6 (R2) Addendum 201...
You are a clinical research professional, investigator, monitor or other staff active in the field o...
You need to update and to refresh your knowledge on the current ICH-GCP E6 (2) and its implement...
Do you know how medical devices find their way to the market? Are you aware that medical applicati...
Investigator Initiated Studies (IIS) are crucial for new product development. These Investigator Ini...
You are a monitor, a project manager or part of an investigator team and need to understand the coun...
Are you a monitor, a project manager or part of an investigator team and need to understand the coun...
How to increase your odds of finding a job in Clinical Research? This STAR Programme will provide...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding of the national regulatory legislation for Clinical ...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
You need a clear and hands-on understanding and be up-to-date of the most current national regul...
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 ...
Clinical Trial Regulations are known to be complex on the one hand, on the other hand, there is no w...
If you are a clinical research professional, investigator, monitor or other staff active in the fiel...
European legislation is often far away from daily life, yet in this interactive eLearn...
The European Clinical Trial Regulation 536/2014, of April 2014, is to become the mandatory unique ru...
This interactive webinar was developed to help you understand the latest elements of the latest vers...