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my professional path as a Project Manager has been varied and progressive in complexity and Leadership.
at a local or country level, i was responsible for clinical study set-up, science)" >Protocol and safety follow-up, and recruitment targets. at a global or sponsor level, i worked articulating cross-functional clinical teams, developing clinical studies in diverse disease areas and having them implemented by local teams. i then expanded my expertise area outside of Clinical Development by becoming responsible for the functional management of global Epidemiology and medical affairs teams. i supervised a team focused on scientific engagement and Market access. since then i also successfully supervised a senior issue management team, supported the Project Management office on the full project costing exercise and delivered Training to newcomers in the team.

my new challenge is now to fully integrate my technical, Leadership and strategic knowledge into value management framework for the measles, mumps, rubella and varicella (mmr,v) program.


Current Experience

  • Senior Program Manager

    Brussels, Belgium
    Since October 2017

    matrix management of cross-functional, multi-disciplinary team.

    Matrix management of cross-functional, multi-disciplinary team.

Past Experience

  • Senior Project Manager

    March 2016 --- September 2017

  • Medical Project Manager Brussels

    January 2014 --- February 2016
    medical affairs key responsibilities: acts as Project Manager. strategic and operational responsibilities apply. ◦ responsible for develop, implement and deliver the cross functional scientific evidence and access plan (seap) ◦ drive execution, coordinate and track progress of project schedule(s) against agreed milestones, costs and resources ◦ develop and update required Budgets and resources for execution of project ◦ ensure that Project Planning information is accurate and up to date in corporate systems used to manage and report progress ◦ drive and foster harmonization in Project Management across medical teams ◦ resolve on a daily basis conflicts between priorities and objectives, between internal players and external experts, between competing projects and between requirements of Compliance Documentation, resources and expediency of activities. Epidemiology key responsibilities: acts as project expediter with managing and recruitment responsibilities. ◦ provide Project Management support to the Epidemiology and Health Economics departments for projects in Discovery and early development phases by contributing to planning development and implementation, and supporting kpi development and metrics collection; ◦ responsible for designing and maintain capacity management for the Epidemiology team; ◦ responsible for the contract development of contingency workers for the Epidemiology team; ◦ contribute to epi budget consolidation by ensuring monthly consolidation and completing benchmarking to redefine new epi activities; ◦ provide overall coordination of the improvements’ and team’s initiatives by adapting epi operating model to new teams and improving contracting process; ◦ be the point of contact for major epi stakeholders in organization.

  • Global Study Manager (Novellas Healthcare consultant)

    October 2010 --- January 2014
    ensures overall operational delivery of the studies according to agreed plans and processes by interacting with all stakeholders to deliver study on time and with quality. the main missions are to lead the operational aspects of the study, to have a thorough knowledge and oversight of all operational study activities (study-set up from science)" rel="nofollow">Protocol design to study start, recruitment follow-up, cleaning, Analysis and reporting timelines), to manage interactions with all stakeholders (study Physician, Data Management, Supply Chain, country managers and CRA,…), to demonstrate Project Manager mindset and apply tools to the study (MS Project, Risk Assessment,…), to relay the voice of the local countries teams at study team level, and to improvement processes.

  • Regional Study Manager (Novellas Healthcare consultant)

    February 2013 --- July 2013
    central management of burden of disease (bod) epidemiological studies in the european region.

  • Product Manager

    June 2010 --- August 2010
    chemical products: antioxidants and organic minerals

  • Clinical Research Associate (CRA)

    January 2010 --- May 2010
    local management of international Phase II Clinical trials.

  • Clinical Research Associate (CRA)

    September 2009 --- December 2009
    local management of international Phase III and iv Clinical trials.

  • Clinical Research Associate (CRA)

    December 2007 --- August 2009
    local management of international Phase II, iii and iv Clinical trials.

  • Clinical Research Associate (CRA)

    January 2007 --- January 2008
    local management of international Phase II and iii Clinical trials.

  • Clinical Data Manager (DM)

    January 2006 --- January 2007
    responsible for international Phase II and iii Clinical trials.

  • Main Analyst Enter Location

    January 2001 --- January 2005
    the Quality Control Laboratory performed Analysis in raw materials, finished products produced by the company customers and company’s own products (manufacture and commercialisation of animal nutraceutics). key responsabilities: - Quality Management - Laboratory management - Microbiology analyses - chemical/physical analyses

  • Chemistry Teacher

    January 2000 --- January 2001

  • Chemistry Teacher

    January 1999 --- January 2000


Self Assessment :
ResiliencyDependabilityOrganizationAssertivenessApproachabilityTrustAuthenticityCommunicativeCoordinationEfficiencyFlexibilityIndependenceProblem solving


Self Assessment :
Project ManagementInformed Consent ProcessMonitoring Study ProgressManaging Clinical Trial SuppliesGood Clinical Practice (GCP)Knowledge of the drug development processCapacity ManagementContractingContingency WorkersQuality ManagementLaboratory Management BiochemistryBiotechnologyCAPAClinical DevelopmentClinical operationsWriting Study Procedures and SOPsVerificationSOPClinical trial managementData ManagementMicrosoft OfficeProblem-solving methods and troubleshooting
LinkedIn Assessment :
PMPProject ManagementClinical trialsClinical researchGCPBiotechnologyICH-GCPChemistryVaccinesCROData ManagementClinical DevelopmentPharmaceutical IndustryClinical monitoringPharmacovigilanceAnalytical SkillsTherapeutic AreasRegulatory submissionsEDConcologyDrug DevelopmentClinical Data ManagementInfectious diseasesContract ManagementMatrix ManagementAnalytical AbilitiesSelf DrivenCommunicativeIssues ResolutionMS ProjectProject ExecutionThought LeadershipFlexibilityReliabilityResilienceLife SciencesCTMSSOPmanagement

Skills and Expertise

Self Assessment :
PMPproject managementBudget managementtime managementScope Manangementchange managementRisk ManagementBusiness strategyBusiness planningBusiness operations


  • Master of Science (MSc) in Applied Chemistry - Biotechnology from Universidade Nova de Lisboa in 1998
  • 12th degree (A-levels) in Natural Sciences from Escola Secundaria Jose Gomes Ferreira in 1992

Training and Certification

  • Project Management PMP® preparation course - Basic + Exam program; Xenturion, Brussels in 2014 Training
  • Manage Others; The Clinical College, Brussels, Belgium in 2013 Training
  • Project Management Professional - PMP® in 2015 Certification
  • Project Management Professional (PMP)® in 0000 Certification


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

Work Preferences

  • Positions I am interested in:
    Project Manager Program Manager (PMP & CSM) Managing Director Associate Director Clinical Operations Business Consultant Global Clinical Project Manager (GCPM, GTM) Global PM Senior Project Manager (PM)
  • Positions I am NOT interested in:
    Clinical Research Associate (CRA) Clinical Project Manager (CPM)
  • Locations I am interested in:
    Antwerpen, Belgique Netherlands
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position :    100% FTE
    BrightOwl employee :    100% FTE
  • International:

Area / Region

Antwerp, Belgium


Driving License
  • Yes

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