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Research engineer and project leader in medical device industry, I am always looking for challenging opportunities that offer room for creativity and innovation with a strengthening internationnal dimension.

» Demonstrated ability to define, analyze, design, develop, and implement innovative diagnostic tool in team environments: - from the idea to the product (e.g. - research, scientific & technical validation, clinical validation, technical implementation, pre-marketting, scientific and medical communication

» Specialized in data mining, statistical modeling, classification, clustering, machine learning (e.g. CART, bagigng, random forest, boosting, svm, neural network, k-NN, k-means, etc.).

» Specialized in biostatistics: hypothesis testing, univariate analysis, ANOVA, regression analysis (multiple linear, logistic, polytomous, ordinal, cox regression) multivariate analysis (PCA, PFA, MANOVA), diagnostic performance analysis, ROC analysis, epidemiology (evaluation of: incidence rates, odds-ratios, relative risks, confounding factors, interaction factors, etc.) .

» Clinical reasearch skills : interaction with physicians and Key-Opinion Leaders, protocol design, case report form design, sample size calculation, monitoring, statistical analysis.

» Medical writing skills : help physicians in writing medical research articles, performing statistical analysis. » Project management skills.

» Team management skills. Management of PhD students, post-doctoral researchers, engineers, biostatistician.

» Communication and research promotion skills : 2 patents, 14 publications, 9 conference articles, 2 chapter books, 80 communications in international conferences. Reviewer for several international medical and scientific papers.

» International work experience: USA, Japan, UK.


Current Experience

  • Senior freelancer & company director
    Since January 2016
    Senior scientist consultant in R&D engineering, project management, data analysis, medical device development, biostatistics, clinical research, medical science liaison, scientific and medical writing Consultant for Echosens:

Past Experience

  • Lead research engineer & project manager
    December 2007 --- December 2015

    2012-2015: lead biomedical scientist and project manager // lead bio-statistician

    2010-2012: senior biomedical scientist and project manager // senior bio-statistician

    2008-2010: biomedical scientist // bio-statistician

    2007-2008: post-doctoral researcher



  • PhD Candidate
    November 2004 --- November 2007

    Data analysis and signl processing for cortical bone characterization.

    Lab instructor, University Paris 12 : Signal Processing, Automatics, Digital Electronics, Office Automation

  • Invited Scientist
    January 2005 --- January 2005
    In vitro characterization of bovine cortical bone

  • Research Engineer
    January 2004 --- January 2004
    Adaptive beamforming in medical ultrasound imaging


Self Assessment :
AdaptabilityAttention to detailCollaborationCommunicativeCreative thinkingCritical thinkingCuriosityEfficiencyFlexibilityInnovative thinkingTrustResult OrientedProblem solvingInterest in knowledgeAnalytical thinking


Self Assessment :
Biostatistics R&D Scientific writingAnalysisBioinformaticsBiomedical EngineeringBiomedical SciencesBusiness IntelligenceClinical researchClinical Study DesignClinical trial designClinical trialsCommunication SkillsCRF designData AnalysisData cleaningData ManagementData ScienceDesign of Experiments (DOE) Developing Clinical Trial ProtocolsDiagnosticsEngineeringEnglishEpidemiologyGrant WritingHealthcare industryKOL managementLaTeXMatlabMedical Device R&DMedical DevicesMedical ImagingMedical writingMetabolismMicrosoft OfficePatentsPhysicsPresentation SkillsProblem SolvingProduct developmentProduct EngineeringProgrammingProject CoordinationProject ManagementProject PlanningProtocolPublic SpeakingRReport WritingRegulatory submissionsResearchSAPscienceScientific CommunicationsScientific methodologyScientific WritingSearch literature on clinical trialsSPSSStatistical Data AnalysisStatisticsStudy protocolsTeachingTeam ManagementTeamworkTechnical reportsTechnological InnovationTechnology DevelopmentTechnology transferTestingUnderstand levels of research evidence
LinkedIn Assessment :
Signal ProcessingBiomedical EngineeringElectrical EngineeringMedical DevicesResearchUltrasoundEngineeringMatlabAlgorithmsCC++R&DTeachingStatisticsMedical ImagingProduct developmentEnglishMicrosoft OfficeLaTeXImage ProcessingImagingAnalysisDigital Image ProcessingData MiningMedical UltrasoundLifesciencesDICOMApplied MathematicsSoftware EngineeringMathematical ModelingProject ManagementDigital Signal ProcessingEmbedded SystemsComputer ScienceMRIPhysicsValidationscienceArtificial IntelligenceRoboticsVideo ProcessingComputer VisionSimulationsDigital ImagingISO 13485Image AnalysisProgrammingMachine LearningDigital Signal ProcessorsSensors

Skills and Expertise

Self Assessment :
Analytical skills Analyze data Control data Develop clinical trial protocols Develop protocols Interpret data Interact with physicians Report data Search literature on clinical trials Design case record forms Technology research Write papers Write protocolsAdvise on strategyAnalyze data/information to determine potential relationships.Attend at steering committee meetingsAttend investigator meetingAttend seminarsAttend seminars, courses and meetings within and outside the companyAttend steering committeebudgeting of R&D activitiescollaborate in research projects at universitiesCollaborate with medical teamCollaborate with principal investigatorCollaborate with project teamCommunicate effectively on different company levelsCommunicate with investigatorCommunicationConduct literature searchesConduct literature searches.Conduct university research Coordinate projectscoordinating research projectsCoordinationCreate clinical documentsData miningData verificationDesign case record form (CRF)Design clinical presentationDesign clinical trialDesign exclusion criteriaDesign inclusion criteriaDesign protocolDesign scientific experimentsDesign studiesDesign study documentsDetermine statistical analysis Develop clinical hypothesesDevelop clinical strategyDevelop protocolsDirect co-workersDirect co-workers to achieve resultEstablish relationships with Key Opinion LeadersEvaluate protocolsExecute scientific projectsFollow up projectsGastrointestinal diseasesGuide studentsGuide staffIdentify investigatorsIdentify risksIdentify sitesIndentify clinicians to conduct clinical trialsInitiate clinical trials Interact with computer specialistsInteract with CROsInteract with KOLInteract with physiciansInteract with pre-clinical scientistsInteract with statisticiansInterpret analytical resultsInterpret dataInterpret research resultsInterpret scientific dataLead studiesLead teamsLiaise with doctorsLiaise with research teamLiaise with professionals in other divisions of the company as requiredLiaise with research team in order to accurately collect and record dataManage multiple projectsManage projects resourcesManage publication strategy of clinical trial resultsManage research projectsmanaging a small teamManuscript preparationManuscript preparation and reviewManuscript reviewMonitor dataObtain grantsOral presentationOrganise meetingsOrganise steering committeeParticipate in medical reviewPeople managementPersuade clinicians to conduct clinical trialsPlan experimentsPlan work to meet objectives and deadlinesPlanning clinical studiesPre-study procedures Prepare final reportPrepare manuscriptPrepare regulatory documentsPrepare responses to health authority queriesPresent clinical resultsPresent data at congressproject managementProvide support for scientific and/or technical projectsProvide trainingPublication of articlesPublish scientific projectsProvide technical supportR&DRead medical literatureRead medical literature to maintain current awareness and knowledgeRegulatory submissionsReview clinical study reportsReview dataReview data interpretationReview medical reportsReview protocolsReview reportsReview study protocolsReview the interpretation of dataSearch literature on clinical trialsSelect contractors Select investigatorsSelect sitesSet up a clinical studySet up research projectsStatistical analysisSupervise data processingSupervise PhD studentsSupervise techniciansTeach university studentsTeachingTranslate clinical research concepts into specific objectivesUnderstand protocolsValidate dataVerify dataWork with coordination and data management teamsWork collaboratively with the other members of the clinical research team Work cross-functionallyWrite clinical evaluation reportsWrite combined statistical and medical reportsWrite documentsWrite final reportsWrite papersWrite statistical reportsWriting regulatory documentsWritten presentation


  • Master's Degree in Public Health from Université Paris Sud (Paris XI) in 2015
  • DU CESAM, Statistics applied in Medicine in Biostatistics from Université Pierre et Marie Curie (Paris VI) in 2012
  • PhD in Biomedical Engineering from Université Paris - Val-de-Marne (Paris XII) in 2007
  • Diplôme d'ingénieur in Signal from Telecom ParisTech in 2004
  • Engineering in Signal processing from Telecom Paris in 2004
  • DU in Research Valorisation in Biomedical Innovation from Université Pierre et Marie Curie (Paris VI) in 2003
  • Engineer in Data analysis and signal processing from Eurecom in 2003

Training and Certification

  • Bayesian statistics in 2017 Training
  • Multi-level statistics in 2017 Training
  • Survival analysis in 2017 Training
  • Statistical modeling in 2016 Training
  • Data mining in 2015 Training
  • Marketting in 2012 Training
  • Biostatistics in 2010 Training
  • Languages

    BrightOwl Assessment:
    Self Assessment:
    Full Proficiency
    Elementary Proficiency
    Elementary Proficiency
    Elementary Proficiency
    Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Biomedical Scientist BioStatistician Clinical Project Leader Data Scientist Engineer Lead Consultant Lecturer Medical Science Liaison (MSL) PhD researcher Principal Scientist Project Leader Project Manager R&D Director R&D engineer R&D manager R&D Scientist researcher Scientific Advisor Scientific consultant Scientific Officer Scientific Researcher Scientific Writer Scientist Senior Consultant Senior Scientist senior research associate Statistician (Consultant)
  • Locations I am interested in:
    London, United Kingdom
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    BrightOwl freelancer :    8 à 16 Hours per week :    30% Free Per Month(in coming months)
  • International:


    Expert has 21 publications (Will be avalible with full profile)

Area / Region

London, United Kingdom


Driving License
  • No