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.
Reasons to attend Clinical Research is one of the most regulated industries in the world. Not a sur...
Reasons to attend Clinical Trial Regulations are known to be complex on the one hand, on the other ...
Reasons to attend This Clinical Research Legislation course is co-developed and given by the Belgia...
Reasons to attend Did you know that your clinical investigations need to comply with the Good Clini...
Reasons to attend This GCP online training is for all those who need to grasp the essence, but not ...
Reasons to attend You want to know where investigational products come from, how they are made an...
Reasons to attend Do you know how medical devices find their way to the market? Are you aware tha...
Reasons to attend Investigator Initiated Studies (IIS) are crucial for new product development. ...
Reasons to attend As a monitor, project manager, or member of an investigator team, it is importa...
Reasons to attend You are a monitor; a project manager or part of an investigator team and you need...
How to increase your odds of finding a job in Clinical Research? This STAR Programme will provide t...
Reasons to attend The Medical Device world is fundamentally different from the Pharmaceutical envir...
Reasons to attend Do you need straightforward instructions on how to write an effective CAPA? Are y...