In good company

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 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 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.

Esther Daemen has over 23 years of experience in the pharma and medical devices sector. She served many organizations in different research roles and as professional development director at ACRP Global. Since 2016, Esther is TRIUM’s Director Quality and Training and since 2018 she acts as the TRIUM ‘Data Protection Manager’. She obtained a bachelor’s degree in nursing, project management and training certificates as well as a master’s degree in business and is a certified DPO. Esther is also a highly-solicited presenter at professional conferences like DIA and writer of peer-reviewed articles for professional magazines like ‘The Clinical Researcher’. Her work was rewarded by the ‘Best trainer to watch’ 2010 Training Magazine Award and the KP-Morgan 2020 ' OECT Summit 10Years Speaker Achievement Award.

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.

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.

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.