
Ms. Liesbeth Lemmens
Trainer
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.

This 4 Day STAR Programme is intended for CRAs wishing to boost their career. As a more experie...
You want to advance your clinical project management skills in order to be more effective in the dyn...
Is your institution faced with an audit/inspection and you want to prepare the team? If so, then thi...
Is your institution faced with an audit/inspection and you want to prepare the team? If so, then thi...

Taking up the responsibility of a clinical trial is dealing with rules and regulations; during this ...
This two-day training for Junior CRAs course will teach you in the basic, yet crucial areas within c...
This series of webinars will train you in the basic, yet crucial areas within clinical monitoring...

Faced with a clinical study and uncertain how to deal with it? This course will take away your doubt...
This course will highlight the steps of the ‘appreciative inquiry’ approach: first investigating...
This is a 1-day course designed to improve your communication skills within the clinical research en...
Did you know that your clinical investigations need to comply with the Good Clinical Practice (GCP...
You are a principal investigator, sub-investigator, study coordinator within clinical ...
Audits and inspections are a fact of life when running clinical trials. This course is design...

You want to know more about auditing and/or the techniques used in GCP-auditing? You do not see the ...
The course is divided into different modules addressing the basic science of oncology, clinical onco...
Investigator Initiated Studies (IIS) are crucial for new product development. These Investigator Ini...
This programme, consisting of 4 course days to be chosen freely from the available dates in the publ...
How to increase your odds of finding a job in Clinical Research? This STAR Programme will provide...
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 ...
Do you feel unorganized? No time to cope with your work? Never reaching deadlines? This course is ma...
This one-day interactive training gives you some hints and tricks on how to improve your training sk...
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