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Team leader and certified project manager with 7 years experience in the R&D pharmaceutical industry to develop innovative vaccines and address significant public health concerns. Demonstrates strategic vision, business needs listening and understanding, leadership skills and the ability to motivate people; Proven track record in project management and cross-functional team management, leading and successfully delivering multiple projects across various phases of vaccines development (Discovery, Clinical and Life-cycle), taking full responsibility and initiative to deliver quality assured results on time.

Career goals
• Contributing to successful development of therapies/prevention that make a difference for the patients
• Develop effective and creative teams in a cross-disciplinary environment
• International mobility



Current Experience

  • Clinical Read-out Team Leader

    Since August 2018
    Clinical trials

    - Manage the clinical assay activities of 4 vaccine programs (Discovery up to life-cycle stage)
    - Develop testing strategies according to the scientific relevance, technical feasibility and regulatory requirements
    - Contribute to writing the scientific and operational parts of clinical trials protocol
    - Lead the clinical assays team and governance to ensure alignment within the project and delivery of data for clinical endpoints
    - Work closely with Experts and Regulatory to address regulatory (FDA, EMA, ..) questions on clinical assays.

Past Experience


Self Assessment :
CollaborationCoordinationCommunicativeCreative thinkingCuriosityEfficiencyFlexibilityInnovative thinkingOptimismProactivityProblem solvingResiliencyResponsibilityResult OrientedSelf-confidenceStrategic thinkingAdaptability


Self Assessment :
Cell biology R&D Phase IAllergy and immunologyAssay developmentBiological Drug DevelopmentBudget ManagementCancerClinical DevelopmentCommunication SkillsCross-functional team leadershipDeveloping Clinical Trial ProtocolsEarly development stageELISAFlow CytometryGood Clinical Practice (GCP)Good Laboratory Practice (GLP)ImmunoassaysImmunologyInfectious diseasesIntegrationInternational Project ManagementISO 9001LaboratoryLaboratory ManagementLeadershipMS ProjectPharmaceutical DevelopmentPhases of clinical development (phase I to IV)Problem SolvingProgram ManagementProject Management

Skills and Expertise

Self Assessment :
Analyze data Analytical skills Develop clinical trial protocols Develop protocols Interpret data Receptor Pharmacology Search literature on clinical trialsAdvise on strategyassess the needs of the project(s)/program(s) and make changes in process, work flow and/or assignments.budgeting of R&D activitiesClinical data collectionCollaborate with project teamContribute medical, clinical expertise and scientific advice to all allied departments in local affiliate in particular support to the local clinical development team for timely execution of studies conducted in the affiliate and to DRA in interactions with authorities.Coordinate projectsCreates a collaborative team environmentDevelop clinical strategyLead teamsproject managementR&DReview clinical study reportsReview protocolsSolve problemsTranslate clinical research concepts into specific objectivesWork cross-functionallyWork collaboratively with the other members of the clinical research team


  • Ph.D. in Biomedical Sciences from ULB in 2010
  • Master in Biomedical Sciences from ULB in 2004

Training and Certification

  • Prince 2 in 2017 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Work Preferences

  • Positions I am interested in:
    Team Leader Manager strategy research Development Manager
  • Locations I am interested in:
    Belgium England, UK France Switzerland United States
  • Work From Home:
    Yes, 0 to 3 days per week
  • Work Regime:
    Permanent position :    100% FTE
  • International:

Area / Region



Driving License
  • Yes


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