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Experiences

Current Experience

  • Associate Director Pharmacodynamics and Translational Medicine


    Since May 2013
    responsible for the scientific activities and Logistics within the molecular medicine and Translational Medicine sections. ensures the activities of the sections are executed at the required quality level within timelines. manages a team of 25 scientists (10 phds) responsible for (pre)Clinical pharmacology Testing. • responsible for resource Planning, timelines, Performance Management, Training and Recruiting • team tasks deal with development of lead drug candidates, including o development, Validation and transfer of potency Assays for drug release and stability Testing o species cross reactivity Testing o demonstration of Preclinical proof of concept in disease models o biomarker Assay development and Validation for (pre)clinical studies o specificity Testing including tissue cross reactivity studies o writing and coordination of a Translational Medicine plan o In Vitro pharmacology TestingMember of multi-disciplinary project teams and Coordinator of departmental project team meetings. contributes to the Strategy of projects. • writing and Editing of regulatory documents (e.g. ib, ind, impd) and participation in regulatory authority meetings e.g. with EMA Responsible for the scientific activities and logistics within the Molecular Medicine and Translational Medicine sections. Ensures the activities of the sections are executed at the required quality level within timelines. Manages a team of 25 scientists (10 PhDs) responsible for (pre)clinical pharmacology testing. • Responsible for resource planning, timelines, performance management, training and recruiting • Team tasks deal with development of lead drug candidates, including o Development, validation and transfer of potency assays for drug release and stability testing o Species cross reactivity testing o Demonstration of Preclinical Proof of concept in disease models o Biomarker assay development and validation for (pre)clinical studies o Specificity testing including tissue cross reactivity studies o Writing and coordination of a Translational Medicine plan o In vitro pharmacology testing • Member of multi-disciplinary project teams and coordinator of departmental project team meetings. Contributes to the strategy of projects. • Writing and editing of regulatory documents (e.g. IB, IND, IMPD) and participation in regulatory authority meetings e.g. with EMA

Past Experience

  • Section Head Pharmacodynamics and Translational Medicine

    May 2010 --- April 2013
    manage a team of 22 scientists (9 phds) responsible for (pre)Clinical pharmacology Testing. • responsible for resource Planning, timelines, Performance Management, Training and Recruiting • team tasks deal with development of lead drug candidates, including o development, Validation and transfer of potency Assays for drug release and stability Testing o species cross reactivity Testing o demonstration of Preclinical proof of concept in disease models o biomarker Assay development and Validation for (pre)clinical studies o specificity Testing including tissue cross reactivity studies o writing and coordination of a Translational Medicine plan o In Vitro pharmacology TestingMember of multi-disciplinary project teams and Coordinator of departmental project team meetings • writing and Editing of regulatory documents (e.g. ib, ind, impd) and participation in regulatory authority meetings e.g. with EMA

  • Senior Scientist Pharmacology

    May 2008 --- April 2010
    manage a team of 15 scientists (4 phds) responsible for (pre)Clinical pharmacology Testing. • responsible for resource Planning, timelines, Performance Management, Training and Recruiting • team tasks deal with development of lead drug candidates, including o development, Validation and transfer of potency Assays for drug release and stability Testing o species cross reactivity Testing o demonstration of Preclinical proof of concept in disease models o biomarker Assay development and Validation for (pre)clinical studies o specificity Testing including tissue cross reactivity studies o In Vitro pharmacology TestingMember of multi-disciplinary project teams • writing of regulatory documents (e.g. ib, ind, impd) and participation in regulatory authority meetings e.g. with EMA

  • Scientist Pharmacology

    January 2006 --- April 2008

  • Post-doctoral Researcher

    February 2006 --- July 2006

  • Post-doctoral Researcher

    October 2003 --- December 2005

Knowledge

LinkedIn Assessment :
pharmacologyBiomarkersAnimal ModelsDrug DevelopmentDrug DiscoveryAssay developmentClinical pharmacologyIn VitroBiopharmaceuticalsBioanalysisAntibodiesPharmacodynamicsTranslational ResearchClinical DevelopmentTranslational MedicineImmunologyMonoclonal AntibodiesProtein PurificationoncologyImmunoassays

Education

  • PhD Biochemistry in Biochemistry from University of Leuven in 2003
  • Licentiaat in Biochemistry from University of Leuven in 1999
  • Kandidaat in Chemistry from University of Leuven in 1997

Area / Region

Kortrijk, Belgium

Others

Driving License
  • No

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