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Experiences

Current Experience

  • Sr. Early Stage Development Scientist


    Since October 2013
    as early stage development Scientist i am managing Phase I Clinical trials in belgium. i manage the local Logistics and am in close contact with investigational sites and investigators. during the clinical part of the clinical studies, i do observational monitoring, data monitoring and source data Verification. i discuss medical issues with investigators to provide my medical colleagues a better insight in the Adverse Events reported by patients. As Early Stage Development Scientist I am managing phase I clinical trials in Belgium. I manage the local logistics and am in close contact with investigational sites and investigators. During the clinical part of the clinical studies, I do observational monitoring, data monitoring and source data verification. I discuss medical issues with investigators to provide my medical colleagues a better insight in the adverse events reported by patients.

Past Experience

  • Jr. Early Stage Development Scientist

    January 2013 --- September 2013

  • PhD student

    January 2010 --- December 2012
    officially i'm a PhD student at this University. due to alliances and expertises in other laboratories, i do my practical work at the vub and cerva-coda-var.

  • PhD student

    January 2010 --- December 2012
    as part of the phd project, and based on the expertise in bacteriophages and Protein Expression, i conduct Laboratory work here, mainly expressing Proteins.

Personality

Self Assessment :
ApproachabilityAttention to detailCharmCreative thinkingCuriosityEfficiencyFlexibilityInterest in knowledgeKindnessProblem solvingTrustWillingness to compromise

Knowledge

Self Assessment :
Phase IClinical monitoringA rising single dose tolerance studyClinical trial managementClinical trialsGood Clinical Practice (GCP)CTMSData entryData cleaningDNA extractionDNA sequencingDrug development processEarly development stageElectronic Data Capture (EDC) ICH GCP guidelinesMicrosoft OfficeMicrosoft ExcelNegotiationPowerPoint
LinkedIn Assessment :
phase I clinical trialsICH-GCPdata monitoringobservational monitoringsource data verificationProject ManagementPositron Emission Tomographymolecular biologyCell CultureProtein ExpressionIn VitroWestern BlottingPCRBiotechnologyELISAMicrobiologyrecombinant DNA technologyProtein PurificationAgarose Gel ElectrophoresisMicroscopy

Skills and Expertise

Self Assessment :
Interact with nurses Interact with physiciansClinical data collectionConduct monitor visitsSolve problems

Education

  • Master's degree in Biomedical/Medical Engineering from Vrije Universiteit Brussel in 2009

Training and Certification

  • PET training in 2015 Training
  • Master in bio-ingeneering in 2009 Certification

Languages

BrightOwl Assessment:
Self Assessment:
Dutch
Native
English
Full Proficiency
French
Professional Proficiency

Work Preferences

  • Notice Period:
    12 weeks
  • Locations I am interested in:
    Belgium Brussels, Belgium
  • Work From Home:
    Yes, 0 to 2 days per week
  • Work Regime:
    Permanent position
    BrightOwl employee
  • International:
    No

Area / Region

Halle, Belgium

Others

Driving License
  • Yes

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