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i am actively looking for new job opportunities with multiple challenges. 


Current Experience

  • Clinical study officer

    Since December 2015
    - support activities and coordination of Clinical research and development programs - scientific and Medical writing - study protocols (ib, icf, crf, SOP...) - contact with principal investigators, site selection and initiation visits - review of Investigator agreement and fees, organization of Investigator/monitor meetings - coordination of monitoring activities - review and support in preparation of regulatory documents/submission files - review of medical literature and related new technologies - Support activities and coordination of clinical research and development programs - Scientific and medical writing - study protocols (IB, ICF, CRF, SOP...) - Contact with Principal Investigators, site selection and initiation visits - Review of investigator agreement and fees, organization of investigator/monitor meetings - Coordination of monitoring activities - Review and support in preparation of Regulatory documents/submission files - Review of medical literature and related new technologies

Past Experience

  • Project Manager R&D

    September 2014 --- December 2015
    Cell therapy from MSc Immunology Clinical Trial environment team manager

  • Post-doctorat

    February 2014 --- August 2014
    intratracheal delivery of lipidic nanocapsules to mice intratracheal delivery of powder broncho-alveolar lavages to perform differential Cell countings and imaging, cytokine and total Protein quantification.

  • PhD student

    October 2010 --- December 2013
    establishemnt of a co-culture of human lung cells and human macrophages Formulation and Characterization of Nanoparticles Cellular Biology tests (toxicity, inflammatory response and Oxidative stress quantification)


Self Assessment :
AdaptabilityInterest in knowledgeAuthenticityCommunicativeCreative thinkingFlexibilityResponsibilityCuriosity


Self Assessment :
Good Clinical Practice (GCP)Good Laboratory Practice (GLP) Cell biologyinflammatory diseasesToxicology
LinkedIn Assessment :
NanoparticlesCell CultureIn Vivoin Vitro ToxicologyFormulationFlow Cytometrypenn-century userMolecular & Cellular BiologyIn VitroNMR spectroscopyMass SpectrometryOrganic SynthesisIR spectroscopyImmunocytochemistryAnimal ModelslungFluorescence MicroscopyNanotechnologyFluorescenceCellCytomIn VitroNanotechnologie

Skills and Expertise

Self Assessment :
Interact with physicians Guide students Search literature on clinical trials Technology research Write papersCell culturecollaborate in research projects at universitiesCollaborate with principal investigatorExecute scientific projectsInteract with ethics committeeInteract with pre-clinical scientists


  • Docteur in Pharmacotechnie et biopharmacie from ED 425 in 2013
  • Diplôme Ingénieur in Chimie-Génie des procédés from ESCPE-Lyon in 2010
  • M2 in Ingénieurie pour la santé et le médicament from UCBL-Lyon 1 in 2010

Training and Certification

  • FELASA in 2016 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency

Work Preferences

  • Notice Period:
    5 weeks
  • Positions I am interested in:
    Biomedical Scientist Medical Science Liaison (MSL) R&D Scientist Scientific Researcher Scientific Writer
  • Positions I am NOT interested in:
    Clinical Project Manager (CPM)
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position
    BrightOwl freelancer
    BrightOwl employee
  • International:

Area / Region

Brussels, Belgium


Driving License
  • Yes

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