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.
LinkedIn Profile
This 4 Day STAR Programme is intended for CRAs, ambitious to further develop their career as a CRA. ...
If you want to advance your clinical project management skills in order to be more effective in the ...
Reasons to attend Is your institution faced with an audit/inspection and you want to prepare the te...
Taking up the responsibility of a clinical trial is dealing with rules and regulations; during this ...
Reasons to attend This course will train you in the basic, yet crucial areas within clinical monito...
Faced with a clinical study and uncertain how to deal with it? This course will take away your doubt...
Reasons to attend This course will highlight the steps of the ‘appreciative inquiry’ approach: ...
Reasons to attend This is a 1-day course designed to improve your communication skills within the c...
Reasons to attend Did you know that your clinical investigations need to comply with the Good Cli...
Reasons to attend You are a principal investigator, sub-investigator, study coordinator within cl...
Reasons to attend Audits and inspections are a fact of life when running clinical trials. Thi...
You want to know more about auditing and/or the techniques used in GCP-auditing? You do not see the ...
Reasons to attend The course is divided into different modules addressing the basic science of onco...
Reasons to attend Investigator Initiated Studies (IIS) are crucial for new product development. The...
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 t...
Reasons to attend Do you need straightforward instructions on how to write an effective CAPA? Are y...
// MicroLearnings are bitesize, online learning activities (eLearning, instructional videos ...
// MicroLearnings are bitesize, online learning activities (eLearning, instructional videos ...
Reasons to attend Do you feel unorganized? No time to cope with your work? Never reaching deadlines...
Reasons to attend This one-day interactive training gives you some hints and tricks on how to impro...