In good company

Mission statement

At TRIUM it's our mission to be a passionate, dedicated business partner with a focus on excellence to provide tailored solutions.

Meet our team

Magdaleen Pieters
Magdaleen Pieters holds a nursing degree, after which she obtained a master degree in hospital sciences as well as a postgraduate master degree in business economics, both at the university of Leuven, Belgium.

Magdaleen has experience in clinical research since 2003 as local and international CRA, project and line manager and clinical operations manager in first-in-human, pre- and post-marketing pharmaceutical and medical device trials.

Inspired by getting the best out of the TRIUM team through authentic and radically human leadership.
Christof Debèfve
Christof Debèfve has obtained a master degree in bio-engineering cell and gene technology as well as a postgraduate master degree in management, both at the university of Leuven, Belgium.

Christof has experience in clinical research since 2004 as local and international CRA, project and line manager in first-in-human trials and pre- and post-marketing pharmaceutical and medical device trials.

Interested in creating change by passionate guidance and authenticity. Currently focusing on business development at TRIUM.
Jan Eelen
Jan Eelen holds a master degree in biomedical sciences as well as a postgraduate degree in biomedical imaging, both obtained at the university of Antwerp, Belgium.

Jan has experience in clinical research since 2000 as local and international CRA, local and international project manager and clinical operations manager in pre- and post-marketing pharmaceutical and medical device trials.

Engaged in process improvement to optimize client satisfaction. Currently focusing on internal operations at TRIUM.
Gijs Klarenbeek
Gijs Klarenbeek has obtained his MD degree at the university of Leuven, Belgium and was trained as a surgeon in the University Hospital of Leuven.

Within the industry, Gijs has experience since 2005 in different medical advisory and management roles. With a background in both pharmaceutical and medical devices context, Gijs has expertise in the cardiovascular and many other therapeutic areas. His medical background and strategic mindset are a significant added value to the team and our clients.

Medical Advisor and Medical Monitor at TRIUM.
Chris De Vos
Chris joined TRIUM with a vast previous expertise in both clinical operations and clinical QA. Former clinical research compliance manager, senior clinical QA auditor as well as ass. director quality monitoring & compliance at J&J.

Subject Matter Expert on compliance at TRIUM.
Anneleen De Cock
Anneleen De Cock holds a Master and a PhD in Movement and Sport Sciences from the University of Ghent, Belgium.

Anneleen has experience in clinical research since 2007 as local and international CRA, local and international project and line manager, clinical program manager and project director in first-in human, pre-and post- marketing medical device and pharmaceutical trials.

Currently focusing on start-up and oversight of TRIUM clinical projects as Project Director.
Isabelle De Bock
Isabelle holds a master in biology and did a 2 year PhD scholarship both at the University of Leuven, as well as obtaining a teacher degree.

She has experience in clinical research since 2003 in operational mgmt. as well as line and team mgmt. in various roles incl. CRA, project manager, resource manager and compliance manager.

Currently leading the Consultancy Solutions at TRIUM.
Bert Peeters
Bert Peeters has obtained a master degree in biomedical sciences as well as a postgraduate degree in management in healthcare, both at the university of Leuven, Belgium.

Bert has experience in clinical research since 2005, with over 10 years of experience in a QA related role, making him a clinical research professional with thorough understanding of clinical trial processes, compliance management and in quality systems including QMS, training, auditing and CAPA management.

Currently responsible for QA and compliance at TRIUM.
Glenn Leemans
Glenn Leemans holds a Master in Rehabilitation Sciences and Physiotherapy, as well as a several certifications in research methodologies and training.

Glenn has experience in clinical research since 2012. He held various research and management roles within the healthcare and medical device industry in combination with academical assignments at the University of Antwerp. His interdisciplinary expertise enables him to skillfully guide the implementation of new therapies and technologies in healthcare by finding the best clinical development route.

Currently responsible for regulatory at TRIUM.

Can we help you?

Contact us
For any question you have related to your clinical research project in the broadest sense, whether you need full project support, expert consultancy, insights on quality, risk-based approaches or need some training, don’t hesitate to contact us. Contact us