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Experiences

Current Experience

  • Director translational medicine

    Luik, Belgium
    Since June 2017

Past Experience

  • Program Leader Diepenbeek

    September 2014 --- June 2017

  • Project Manager Brussels, Belgium

    July 2014 --- September 2014
    • provide support in the selection process of appropriate subcontractors (i.e. cros and cmos) for the execution of the planned cmc activities, Preclinical studies and the future Clinical studies
    • support the design of cmc, Preclinical and Clinical study plans in close collaboration with consultants assigned to the project
    • manage the approved study plans, timelines and budget with the selected subcontractors, from initial panning to final reporting

  • Scientist Pharmacodynamics/Translational Medicine Zwijnaarde, Ghent, Belgium

    July 2011 --- July 2014
    • act as department representative at cross-departmental and stakeholder management meetings
    • management of team of associate scientists and (sr.) Research associate
    • supervision of (sr.) research associates
    • organizer, moderator and Coordinator of departmental project meetings
    • active Member of the oncology-focus group responsible to identify potential new target to initiate internal research programs in oncology
    • responsible for establishing relationship/collaboration with kols and CRO
    • responsible for outsourced In Vivo pre-Clinical studies with CRO (identification, contracting, study science)" rel="nofollow">Protocol, study monitoring and reporting)
    • define strategies for In Vivo proof of concept determination in disease models
    • involvement in partnering discussions as lead Scientist for specific projects
    • determination of Translational Medicine Strategy for lead compound
    • development and Validation of Biomarker Assays for pre-Clinical studies

  • Post-doctoral scholar Chicago, IL, United States

    August 2009 --- February 2011
    • lead and implement scientific projects focused on tumor microenvironment (during ovarian and breast cancers).
    • design, implement and complete Research projects.
    • review and interpret scientific and medical literature, publish and present data at national and international conferences and in internationally recognized journals
    • write successful Applications to obtain Research funds and scientific manuscripts.
    • perform scientific experiments and trouble-shoot related problems.
    • review scientific and medical literature.
    • train and supervise phd, master students and technicians.

Personality

Self Assessment :
Analytical thinkingAssertivenessAttention to detailCollaborationCommunicativeCompetitivenessCreative thinkingCritical thinkingCuriosityCoordinationEfficiencyIndependenceInterest in knowledgeOptimismOrganizationResponsibilityResult OrientedFlexibilityInnovative thinkingProactivityStrategic thinkingWillingness to compromiseSelf-confidence

Knowledge

Self Assessment :
Animal models Cell biology Negotiation R&D Scientific writingAllergy and immunologyAnalytical techniquesAntibodiesBiological Drug DevelopmentBiomarkersBiopharmaceuticalsBiotechnologyBudget ManagementCancerCell biologyCell CultureCommunication SkillsCross-functional team leadershipContract negotiationDrug development processEarly development stageEnglishELISAFlow CytometryImmunocytochemistry (ICC)Immunohistochemistry (IHC)Grant Writinggrant writing and designIn VitroIn VivoKnowledge of the drug development processKOL managementLaboratory ManagementMicrosoft ExcelTime ManagementTeam LeadershipSearch literature on clinical trialsScientific WritingR&DProduct developmentPre-clinical researchoncology

Skills and Expertise

Self Assessment :
Supervise technicians Report data Interpret data Search literature on clinical trialsBiomarker Researchbudgeting of R&D activitiesDirect co-workersExecute scientific projects

Education

  • PhD in Oncology from Vanderbilt University in 2009

Languages

BrightOwl Assessment:
Self Assessment:
English
Full Proficiency
French
Native

Work Preferences

  • Positions I am interested in:
    Project Leader R&D Director translational medicine biomarker
  • Locations I am interested in:
    Flemish Brabant, Belgium Leuven, Belgium Wavre, Belgium
  • Work From Home:
    Yes, 1 to 3 days per week
  • Work Regime:
    Permanent position :    100% FTE
  • International:
    Yes

Area / Region

Kessel-Lo, Belgium

Others

Driving License
  • Yes

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