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Experiences

Current Experience

  • Research Physician


    Since January 2015

Past Experience

  • Clinical Study Researcher

    December 2013 --- October 2015

  • Research Physician, R & D Hartteam

    April 2012 --- April 2013

  • Research Physician

    August 2009 --- April 2012
    developing Research proposals with a focus on the effects of lifestyle interventions on Inflammation regulating mechanisms. responsible for scientific / medical aspects in all trials with volunteers.

  • Research Physician/ Project Manager

    January 2004 --- January 2009
    management of various projects with a focus on thermo-Physiology, exercise and aviation Medicine. responsible for scientific / medical aspects in all trials with volunteers.

  • Research Physician / Project Manager

    January 1997 --- January 2004
    managing Research projects investigating Health effects of functional foods (Budgets up to 3 million €). responsible for scientific / medical aspects in all trials with volunteers

  • Clinical Research Scientist

    January 1995 --- January 1997
    coordination Clinical trials

  • Clinical Research Physician

    January 1993 --- January 1995
    medical information officer post Marketing surveillance medical Training Sales department coordination Clinical trials

Personality

Self Assessment :
Attention to detailCreative thinkingCuriosityCritical thinkingFlexibilityInnovative thinkingProblem solving

Knowledge

LinkedIn Assessment :
Clinical researchPublic HealthLife SciencesHealthcareMedical DevicesClinical trialsResearchClinical DevelopmentScientific WritingImmunologyR&DLifesciences

Skills and Expertise

Self Assessment :
Develop clinical trial protocols Guide students Interact with nurses Interpret data Search literature on clinical trialsAdjust processes and methodsAdverse event reportingApprove patient informationAssess adverse reactionsAssess business and scientific ethicsAssess site feasibilityAssess subject safetyassess the needs of the project(s)/program(s) and make changes in process, work flow and/or assignments.Assure medical qualityAttend investigator meetingAttend steering committeeBiomarker Researchbudgeting of R&D activitiesCalculate timelines for conducting and completing the trialCapture data on source documentsClinical data collectionCoach and provide guidance to clinical staff.collaborate in research projects at universitiesCommunicate with sponsorCommunicate with investigatorComplete case report form (CRF)Complete study proceduresConduct limited data and/or statistical analysis.Conduct literature searchesConduct studiesConduct research at universitiesCoordinate with the ethics commiteeCoordinate projectsCreate clinical documentsCreate SOPsDesign clinical trialDesign inclusion criteria

Education

  • PhD in PhD Research from Maastricht University in 1994
  • MD in Medicine from Leiden University in 1987
  • in Liberal Arts and Sciences from Linfield College in 1979
  • in Atheneum b from Paulus Lyceum, Tilburg in 1978

Languages

BrightOwl Assessment:
Self Assessment:
Dutch
Native
English
Professional Proficiency
French
Elementary Proficiency
German
Elementary Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Positions I am interested in:
    Associate Director Clinical Operations Clinical Research Physician Drug Safety Officer Medical Advisor Medical Director Medical Officer Scientific Advisor Scientific Officer
  • Work From Home:
    No
  • Work Regime:
    Permanent position :    100% FTE
    BrightOwl freelancer :    32 Hours per week
  • International:
    Yes

Area / Region

Bosch en Duin, Netherlands

Others

Driving License
  • Yes

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