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 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 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 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.
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.
Anneleen De Cock
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
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 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 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.