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Director in Clinical Pharmacology with more than 20 years experience in the management and conduct of early phase trials in different therapeutic areas and European countries. Managed +/- 30 studies per year (First-in-Man, Experimental Medicine, Exploratory, Proof-of-Concept, Pharmacodynamic/Biomarker studies, Patient studies,...). Experience in project management. Experience in GMP requirements for early phase trials. Setup of QA systems for drug supplies management.


Current Experience

  • Founder & Owner
    Since February 2011
    Consultancy in Clinical Operations Early Development Project Management all clinical phases Experience in different therapeutic areas Business development Training

Past Experience

  • Consultant Clinical Operations
    October 2010 --- January 2011
    Global Clinical Operations including Early phase trials, Late phase trials,Project management

  • Director Clinical Pharmacology Europe
    January 1990 --- March 2010
    Management of early phase studies (Phase I, Ib, IIa studies, Exploratory trials, Expermintal Medicine studies) in different therapeutic areas (diabetes, obesity, CNS, infectious diseases, cardiovascular diseases,etc..) and in different European countries.


LinkedIn Assessment :
Clinical researchInfectious diseasesTherapeutic AreasDiabetesClinical pharmacologyMedicineGMPQuality Assurance (QA)Clinical trialsClinical DevelopmentPharmaceutical IndustryoncologyClinical operationsBiotechnologyLifesciencesPhase I


  • PharmD, PhD in Therapeutic drug monitoring from Vrije Universiteit Brussel in 1988

Area / Region



Driving License
  • No