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Current Experience

  • Global Programme Manager, Biologics

    Munich, Germany
    Since June 2014
    Clinical Development

    • Responsible for overarching coordination, control and completion of global cross‐functional biologics / biosimilars development projects in house, at contract service providers and in collaboration with other pharma and biotech companies. • Lead cross-functional strategic and operational development plans for a portfolio of biosimilar programs. • Lead international multidisciplinary programme team and the process of decision-making within the projects. • Contribute to key activities working with functions (Technical Development, Operational Planning, Pre-Clinical & Clinical Development, Regulatory Affairs, Intellectual Property, In Vitro / Companion Diagnostics) to ensure excellence in planning, budget forecast, decision making, risk management and communication. • Consolidate cross-functional programme information for reporting to steering committee and board. • Responsible for project budgets of assigned development projects of € 80‐100 M

Past Experience

  • Director, Technology Development & Antibody Engineering Grenoble & Lyon, France

    January 2010 --- May 2014
    Business Development

  • Assoc Director, Biotherapeutics Development

    January 2008 --- January 2010
    Assay development

  • R&D Director London, United Kingdom

    May 2004 --- January 2008
    Due Diligence

  • Team Leader/Project Manager London, United Kingdom

    December 2001 --- April 2004


LinkedIn Assessment :
Monoclonal AntibodiesBiotechnologyMammalian Cell CultureProtein EngineeringTechnology transferProtein chemistryBioprocessProject Portfolio ManagementAntibodiesCellBiochemistryImmunologyTeam BuildingUpstream processingAssay developmentStrategic PlanningDrug DiscoveryProcess SimulationGMPHigh Throughput ScreeningCross-functional team leadershipProtein ExpressionBiomarkersLife SciencesPharmaceutical IndustryBiopharmaceuticalsCell CultureDrug DevelopmentInfectious diseases

Skills and Expertise

Self Assessment :
biologicsbiosimilarsAttend steering committeebudgeting of R&D activitiesContract approvalCoordinate projectsDirect co-workersEstablish contractsExecute scientific projectsFollow up projectsIdentify risksInteract with CROsInteract with regulatory stakeholdersLead teamsLiaise with professionals in other divisions of the company as requiredManage budgetsManage complexityNegotiate budget NegotiationOrganise meetingsOrganise steering committeePrepare regulatory documentsproject managementPublish scientific projectsRead medical literatureRegulatory documentationReview protocolsReview study protocolsSelect contractors Support due diligence assessments


  • Research Associate in Department of Biological Sciences from Imperial College London in 2006
  • Certificate in First Line Management in from Institute of Leadership and Management, UK in 2005
  • Post Doctoral Research in Department of Immunology and Molecular Pathology from UCL in 2001
  • BSc, MSc, PhD in Biochemistry from The Hebrew University in 1996


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Work Preferences

  • Locations I am interested in:
  • Work From Home:
  • Work Regime:
    Permanent position
  • International:

Area / Region

London, United Kingdom


Driving License
  • No

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