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I am looking for a high level job in the pharmaceutical Industry. I have worked at UCB and discovered Keppra, GSK Bio (vaccines) and JNJ R@D (small molecules. I am Senior and speak English, French and Dutch and have understanding of German. I did postdoctural research in Japan and know the Japanese culture and tradition. I have about 200 articles in international journals and am looking for a jovb such as CEO, Head of Medical Department, Regulatory Affairs or Toxicology (with a MSc Degree at the University of Surrey, UK). I am available. 

My expertise is in development of vaccines or small molecules in Infectious Diseases (including HIV), Oncology and Toxicology. I also have experience in registration of novel compounds in US, EU and Japan. 


Current Experience

  • Senior Director Medical Lead

    Mechelen, Belgium
    Since February 2017

Past Experience

  • Senior Director Early Development Mechelen, Beerse, Belgium;

    April 2002 --- January 2017

  • Associate Director Regulatory Affairs SB Immunotherapeutics and later Director Reg Affairs , GSK Biologicals Rixensart, Belgium

    May 1997 --- March 2006

  • Head of Zootechnical department, Tox department and member of EC UCB SA, Braine-L'Alleud, Belgium

    September 1989 --- March 1996

  • Head of Pharmacological Screening UCB SA, Braine-l'Alleud, Belgium

    September 1985 --- September 1988

  • Head of Cardiovascular Biochemistry UCB Brussels

    September 1983 --- September 1985


Self Assessment :
CommunicativeCreative thinkingEfficiencyInnovative thinking


Self Assessment :
Animal models Diabetes Biochemistry Phase I R&D Scientific writingAdverse Events (AE)Allergy and immunologyAntibodiesBiological Drug DevelopmentBiomedical SciencesBiotechnologyCancerClinical DevelopmentClinical pharmacologyClinical trial designDrug Safety and PharmacovigilanceeCTDFDAFlow CytometryGeneral MedicineGood Clinical Practice (GCP)Good Manufacturing Practice (GMP)ICH guidelinesImmunologyNanomedicineNeuroscienceoncologyOncology Clinical Research

Skills and Expertise

Self Assessment :
Assure medical quality Develop clinical trial protocols Interact with physicians Write papersClinical data collectionCommunicate with investigatorCommunicate with sponsorConduct site initiationConduct the trialControl protocol versionsDesign clinical trialDesign inclusion criteriaDesign exclusion criteriaDesign protocolsDevelop regulatory strategyEthics committee submissionsEvaluate licensing opportunitiesExecute scientific projects


  • Master Degree in Safety Assessment and Applied Toxicology in Toxicity studies in animals and in vitro from University of Surrey, Guildford in 1993
  • Doctor of Medicine in Medicine from Free University of Brussels in 1983
  • PhD in Biochemistry in Biochemistry/immunology from Free University of Brussels in 1979

Training and Certification

  • Training in Pharmac. Development and Chemical Safety, Polytechnic of East London, UK in 1992 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Professional Proficiency
Elementary Proficiency
Elementary Proficiency


    Expert has 1 publications (Will be avalible with full profile)

Area / Region

Ternat, Belgium


Driving License
  • Yes

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