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Clinical Research and Development Lead in vaccines with experience in Project management, Scientific writing and Data management and with a PhD in Sciences (Molecular biology). Expertise in different therapeutic areas (Immunology, ophtalmology, nutritional and metabolic diseases, gastroenterology, diabetes, cardiovascular diseases).


Current Experience

  • Clinical Research and Development Lead at GSK Vaccines – Zoster studies
    Since December 2016

Past Experience

  • Clinical trial coordinator
    July 2016 --- November 2016

  • Clinical Project Leader
    September 2014 --- June 2016
    Clinical project management activities: - Project management: planning, contracts, budget, regulatory submissions (IEC, RA) - Coordination of monitoring, data management, statistical and scientific writing activities - Communication with sponsor, investigational sites, service providers, regulatory authorities - Translation: French to English and English to French - Review of study documents: protocol, CRF, SAP, monitoring plan … Scientific writing activities: - Review of statistical tables and presentation of study results - Writing: clinical study documents, Clinical Study Reports, publications, posters, powerpoint presentations Data Management activities: - CRF review, database design, Data Validation Plan, quality checks programming and validation, data cleaning - Participation to Data Review meetings

  • Intern
    July 2014 --- September 2014
    Intern at the DG PRE authorisation - Marketing authorisation - Centralised Procedure. Learning of: - Management of applications for the centralised procedure (and support of CHMP members) - European pharmaceutical legislation concepts - Registration procedures (Centralised, decentralised, mutual recognition and national procedures) - Organisation and operation of the European Medicines Agency (EMA) - Organisation and operation of the Federal Agency for Medicines and Health Products (FAMHP – Belgium)

  • Clinet training
    March 2014 --- May 2014
    Clinical research trainings: - Medical writing - Regulatory affairs - Pharmacovigilance - Quality assurance - GLP, GMP, GCP - Data management - Biostatistics - Health economic - Drug development - Pharmacokinetics and drug metabolism

  • PhD in Sciences
    January 2007 --- January 2013
    Laboratory: Unit of Biochemistry and Molecular Genetics of Bacteria, Institute of Life Sciences, UCL Aim of the project: Regulation of competence for natural transformation in Steptococcus thermophilus Expertise domains: molecular biology, transcriptomic, DNA transfer, SOS response, bacteriology, biochemistry


Self Assessment :
CuriosityInterest in knowledgeCritical thinkingProblem solvingAttention to detailResult OrientedProactivity


Self Assessment :
ICHElectronic Data Capture (EDC) Project ManagementEMAClinical Data Management (CDM)CROGood Clinical Practice (GCP)MedDRAVaccines
LinkedIn Assessment :
Clinical researchScientific WritingData ManagementGCPSciences de la vieGeneticsTranscriptomicBiologie molBiotechnologieBacteriologyBiochemistryMicroarrayGene RegulationSupervisory ExperienceScientific AnalysisRegulatory affairsDrug DevelopmentBonnes pratiques cliniquesClinsightSQLGMPGLPLife SciencesRegulatory AgenciesClinical study reportCTMS

Skills and Expertise

Self Assessment :
Analyze data Build and manage the Trial Master File (TMF) Control data Design case record forms Develop clinical trial protocols Guide students Interpret data Interact with nurses Interact with physicians Molecular Diagnostics Report dataApprove monitoring reportsCommunicate with investigatorCommunicate with sponsorConduct research at universitiesDesign database Written presentationWriting regulatory documents Monitor a clinical studyWrite combined statistical and medical reportsWrite protocolsWrite papersRegulatory submissionsPublication of articlesCoordinate projectsManage clinical trial files/documentsR&D


  • PhD in Sciences in Molecular Biology from Université catholique de Louvain in 2013
  • Master's degree in DEA-Advanced master in sciences (biology) from Université catholique de Louvain in 2007
  • Master's Degree in Biology (Molecular, cellular and human biology) from Université catholique de Louvain in 2005

Training and Certification

  • Access 2010 in 2014 Training
  • Clinet Training in 2014 Training
  • Conception de bases de données in 2014 Training
  • MySQL fundamentals in 2014 Training
  • Certificat de formation à la recherche en Sciences Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Elementary Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Locations I am interested in:
    Belgium Lille, France
  • Work From Home:
    Yes, 0 to 2 days per week
  • International:


    Expert has 5 publications (Will be avalible with full profile)

Area / Region

Tournai, Belgium


Driving License
  • Yes