BrightOwl Loader Loading


Degrees: MD and PHD in Biomedical science and pharmaceuticals

Working experiences: Clinical research and Development lead (GSK Vaccine), Clinical project manager (EORTC)

Personalities: determined, mature, motivated, creative,


Current Experience

  • Clinical Research and Development Lead Wavre, Belgium
    Since January 2013

    Leading the clinical team at GSK Vaccine, responsible for scientific and medical oversight of the clinical studies (including GCP, data quality and budget aspects).

Past Experience

  • Clinical Project Manager (CPM) Brussels, Belgium
    June 2010 --- June 2011
    Clinical study oversight on operational aspects (quality, timelines, budget, logistics etc)

  • Post doc researacher Brussels, Belgium
    January 2010 --- May 2010

    Post doc researcher on Diabetes

  • Teacher Beijing, PRChina
    September 1997 --- June 2001
    Lecturing to undergraduate students on Women and Children's health


Self Assessment :
Self-confidenceCreative thinkingDiligenceOrganizationSelf-discipline


Self Assessment :
Phases of clinical development (phase I to IV)Clinical researchVaccinesClinical trialsClinical DevelopmentClinical operationsClinical trial designMedical writingProtocolscienceScientific WritingProject Management

Skills and Expertise

Self Assessment :
Act as the main line of communication between the sponsor and the investigatorAdminister, maintain and co-ordinate the logistical aspects of clinical trialsApprove suitability of patient information and consent documentsAssess subject safety during trialAttend seminars, courses and meetings within and outside the companyCoach and provide guidance to clinical staff.Create clinical strategies for developing investigational drugs to the point of market approvalDesign the studyDevelop protocolsDirect co-workers to achieve resultDiscuss the results of testing with medical statisticiansEnsure all clinical trials are executed in compliance with international GCP guidelines/regulations and SOPsEvaluate, review and assess protocols and amendments for subject safety and welfareExtrapolate resultsInteract with statisticiansInterpret dataParticipate in meetings with sponsors, monitors and regulatory authorities, as necessary.Plan and coordinate regular advisory board and steering committee meetings.Write protocolsRead medical literature to maintain current awareness and knowledgeManuscript preparation and reviewR&D


  • PhD in Biomedical Science and Pharmaceuticals from ULB, Brussels in 2009
  • Master of Science in Biomedical Sciences, Major in Research in Molecular Biology and Biotechnology from VUB, Brussels in 2002
  • Bachelor in MD from Beijing Medical University in 1997

Area / Region

Etterbeek, Brussels, Belgium


Driving License
  • Yes