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Proven sales and marketing experience as well as: clinical introduction support and development, research and data gathering and it's management through training, experience, perseverance and fortitude. • Clinical Project Manager in a wide variety of business applications. • Experienced hands-on product development skills. • Interested in early-stage startups as well as companies “on the bubble.” • Training and introduction experience in the medical device market. • Expanding clinical applications and indications for use. • Intermediate between the clinical arena and the product development team. • International experience with the different languages and cultures en sales en marketing Specialties: Training, introduction of new devices on the market, clinically support the new device introduction, pick up ‘the good the bad and the ugly’ from the clinical arena and translate that to the device development team. Clinically support the hands-on training of the operator and the hospital staff. Organization of registries and randomized trials. Iso and CE registration. Setting up a worldwide distribution and sales agent network


Current Experience

  • Clinical Field Engineer

    Since November 2016
    Clinical Trial

    Participate in all aspects of the conduct of clinical trials at assigned
    sites and support the enrolment at specific clinical sites.
     Data collection during clinical trial procedures
     Generate and maintain working relations with the investigators and the research staff at the clinical sites.
     Assist in the management of the of the clinical site monitoring plans and procedures.
     Assist in maintaining clinical site compliance.
     Serve as clinical trial and the protocol expert, ensuring each site’s protocol compliance.
     Consistently promote collaboration positivity, accountability, and resourcefulness.
     Work closely with the departmental personnel on the status of the of assigned sites for all clinical trials.
     Oversee and or conduct site initiation and staff and investigator training.
     Provide feedback to management on the ongoing, progress of assigned site for all clinical trials

  • General Manager

    Since December 2012

    Alja Lambers and Hand Meulenbrug founded the company in 2012. Due to their experience over the past 20 years they developed a fast network of professionals. core business: Clinical sales and marketing, investment, support and develop new modalities, products and ideas to market

Past Experience

  • Account manager Dach Benelux and CE Leiden

    January 2016 --- June 2016
    Medical Imaging

  • CEO/General Manager

    April 2003 --- July 2015

  • Clinical Marketing Consultant Oxford, Verenigd Koninkrijk

    July 2014 --- July 2015

  • Consultant

    April 2003 --- November 2006

  • Clinical Director

    February 2002 --- February 2003

  • Clinical Director

    January 2000 --- September 2002

  • Clinical Training Manager Europe

    December 1997 --- January 2000

  • Clinical Manager Europe

    January 1995 --- January 1997

  • Clinical Specialist Europe Middle East and SA

    January 1990 --- July 1995

  • Nurse IC ICU

    March 1986 --- September 1990

  • General Nurse

    September 1981 --- February 1986


BrightOwl Assessment :
Service orientedAssertivenessImpulse commandAnger commandApproachabilityPerspectiveProblem solvingAnalytical thinkingDependabilityOrganizationAuthenticityCreative thinkingInterest in knowledgeCuriosity
Self Assessment :
SociabilityTrustStrategic thinkingSelf-disciplineOrientationCuriosityCompetitivenessIndividualityCreative thinkingCollaborationCharmAuthenticityAttention to detailAssertivenessApproachabilityAnalytical thinkingCritical thinkingCoordinationProblem solvingKindnessOrganizationOptimismInterest in knowledgeIndependenceInnovative thinkingEfficiencyAdaptability


BrightOwl Assessment :
Medical Devices R&DCardiologyHospitalspeople managementProblem-solving methods and troubleshootingProduct designProject ManagementPulmonary diseasesRespiratoryTeam Leadership NegotiationPatient Screening and RecruitmentProcess improvement
Self Assessment :
Animal models Diabetes Medical devices Negotiation Phase I R&D Scientific writingAnesthesiaAnimal trialAnimal ModelsCardiologyCardiovascular diseasesClinical Data Management (CDM)Clinical DevelopmentClinical monitoringClinical operationsClinical researchClinical Study DesignClinical trial audits and inspectionsClinical trial budgetingClinical trial designClinical trial managementClinical trialsContract negotiationData ManagementData entryData AnalysisDesigning case report formsDiagnostic radiologyEnglishEthics submission and approval processFDAGermanGood Clinical Practice (GCP)HospitalsHuman ResourcesKOL managementManaging Clinical Trial SuppliesMarket accessMedical affairsMedical budget managementMedical consultingMedical DevicesMedical writingMicrosoft ExcelMicrosoft OfficeMonitoring Study ProgressNegotiationpeople managementPhases of clinical development (phase I to IV)PowerPointPrinciples and ethics of clinical researchProduct launchProject ManagementProtocolPulmonary diseasesR&DRegistration of the productWriting Study Procedures and SOPsInformed Consent DocumentsUnderstanding of regulatory guidelinesThoracic surgeryTechnical reportsTeam LeadershipSupervising CRAsRegulatory affairsQuality Assurance (QA)Product designPre-clinical researchPreclinical regulations and practicesPatient Screening and Recruitment
LinkedIn Assessment :
CardiologyClinicalInterventional CardiologyProduct developmentClinical DevelopmentClinical researchNew Business DevelopmentCapital EquipmentMedical DevicesStart-upsMarket developmentProduct launchHealthcareCommercializationHospitalsGlobal Marketing

Skills and Expertise

BrightOwl Assessment :
Interact with nurses Interact with physicians Interpret data Search literature on clinical trials Technology researchAdjust methodsAdjust processes Adjust processes and methodsAdvise on medical perspectivesAssist with proceduresAssist with routine testsAssure medical qualityCoachCoach clinical staffCoach staffCollaborate with medical teamCollaborate with project teamConduct literature searchesCreates a collaborative team environmentDirect co-workersExecute scientific projectsGuide staffInteract with physiciansInterpret dataLiaise with doctorsLiaise with research teamlifescienceNegotiationNetworkProvide input to process improvement initiativesRead medical literatureSolve problemsTrain on site staff
Self Assessment :
Monitoring enrolmentLiaise with doctorsInterpret dataInteract with pre-clinical scientistsInteract with physiciansInteract with nursesInteract with ethics committeeInteract with CROsInformed consent processIdentify investigatorsLiaise with research teamIndentify sitesMonitor dataMonitor clinical trials Monitor a clinical studyManuscript preparation and reviewManage study budgetManage projects resourcesManage contractors Manage Clinical Trial Management System (CTMS) Manage clinical trial files/documentsIndentify clinicians to conduct clinical trialsImplement data collection systemEnsure data consistencyDocument data reporting systemsDocument data collection systemDocument adverse eventsDistribute trial suppliesDistribute study documentsDiscuss treatments with investigatorDirect co-workersDevelop study timelinesEnsure data integrityEnsure good clinical practice (GCP)Handle callsGuide staffFacilitate sponsor monitoring visitsExtrapolate dataExecute scientific projectsEvaluate protocolsEthics committee submissionsEthics committee applicationEstimate subject complianceDevelop study budgetMonitoring subject complianceScreen patientsValidate dataWrite medical reportsWrite papersWritten presentationReview study protocolsReview monitoring reportsReview exclusion criteriaReview inclusion criteriaReview medical reportsTrain on site staffTrain off site staffSelect contractors Select investigatorsSet up a clinical studySite managementSolve problemsSupervise clinical monitorsSupervise data processingSupervise techniciansSupervise trial suppliesResearch at universitiesReport serious adverse events (SAE)Patient liaisonParticipate in medical reviewOrganise steering committeeOrganise meetingsOral presentationOffice managementNegotiationNegotiate protocol details Negotiate payment schedulesPatient recruitmentPersuade clinicians to conduct clinical trialsRead medical literaturePublish scientific projectsPublication of articlesProvide trainingProtocol managementPromotional materialsPresent clinical resultsPresent data at congressPlanning clinical studiesNegotiate budget Develop regulatory strategyComplete case report form (CRF)Attend steering committeeAttend seminarsAttend investigator meetingAssure medical qualityAssist with routine testsAssist with experimentsAssist with proceduresAssist study siteAssign activitiesClinical data collectionCoachCommunicate with sponsorCommunicate with investigatorCollect patient forms and questionnairesCollect financial data from hospitalsCollaborate with project teamCollaborate with principal investigatorCollaborate with medical teamCoach staffCoach clinical staffAssess subject safetyAssess site feasibility Report data Monitor a clinical study Interpret data Interact with physicians Interact with nurses Guide students Develop protocols Develop clinical trial protocols Design case record forms Search literature on clinical trials Technology researchAssess adverse reactionsArchive documentationApprove queriesApprove patient informationApprove monitoring reportsApprove consent documentsAnalyze dataAdvise on medical perspectives Write papers Assure medical qualityComplete study proceduresDevelop clinical trial protocolsDesign information leafletDesign inclusion criteriaDesign exclusion criteriaDesign data reporting systemsDesign data collection systemsDesign Clinical Trial Management System (CTMS) Design clinical trialDesign case record form (CRF)Data validationDesign marketing advertismentsDesign post-marketing surveillance studyDevelop clinical strategyDevelop clinical hypothesesDetermine potential relationshipsDesign trial master file (TMF)Design tracking systemDesign subject consent formDesign study documentsDesign studyDesign protocolData verificationData entryContact potential subjectsConfirm protocol complianceConduct university research Conduct the trialConduct site initiationConduct research at universitiesConduct post-marketing surveillance studyConduct monitor visitsConduct literature searchesContract approvalCoordinate ethics committeeCreate study documentsCreate standard operating procedure (SOP)Create SOPsCreate economic parametersCreate clinical documentscoordinating research projectsCoordinate with the ethics commiteeCoordinate regular advisory boardCoordinate logisticsConduct close-out visits


  • in Marketing from NIMA-A in 1995
  • RN in Intensive care Coronary care from Fontys Hogescholen in 1988
  • RN in General nursing from Nursing School Eindhoven in 1984
  • Bachelor of Science (BSc) in from Osteopathie College Sutherland in 0000

Training and Certification

  • NIMA A in 2003 Certification


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

Work Preferences

  • Notice Period:
    1 week
  • Work From Home:
    Yes, 0 to 5 days per week
  • International:


    Expert has 3 publications (Will be avalible with full profile)

Area / Region

Achlum, Nederland


Driving License
  • Yes


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