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Summary

 

Personality

BrightOwl Assessment :
Impulse commandPerspectiveKindnessAnalytical thinkingAttention to detailCollaborationCoordinationCreative thinkingCritical thinkingOrganizationProblem solvingWillingness to compromise
Self Assessment :
AdaptabilityProblem solvingTrustWillingness to compromiseResiliencyAttention to detailAnalytical thinkingCharmCollaborationCreative thinkingDiligenceCritical thinkingEfficiencyIndependenceKindnessOptimismOrganization

Knowledge

BrightOwl Assessment :
NegotiationContract negotiationProblem-solving methods and troubleshootingLegal Considerations: Contracts and IndemnityPhases of clinical development (phase I to IV)Project ManagementdutchHospitalsClinical monitoringInterpret clinical trial resultsScientific methodology
Self Assessment :
Family practiceFDAFlow CytometryGastroenterologyGCPGeneral practiceGeneticsGood Clinical Practice (GCP)GermanHematologyHospitalsICH GCP guidelinesICH-GCPIMPDInflammationInformed Consent ProcessLegal Considerations: Contracts and IndemnityManaging Clinical Trial SuppliesContract negotiationMicrosoft OfficeMicrosoft ExcelMonitoring Study ProgressNegotiationoncologyOperating RoomPatient Reported Outcome Measures (PROMs)PathologyPatient Follow UpPatient Screening and Recruitmentpeople managementPharmaceutical IndustryPharmacodynamicsPharmacogeneticsPharmacogenomics (study of genetic variation)PharmacokineticsPharmacovigilancePhase IIPhase IIIPhase IVPhases of clinical development (phase I to IV)Phenotype PowerPointProblem-solving methods and troubleshootingPrinciples and ethics of clinical researchProject ManagementProtocolPsychiatryPulmonary diseasesQualificationQuality Assurance (QA)Quality of Life (QoL) outcomesRadiation oncologyRandomization and blindingRegulatory RequirementsRegulatory submissionsSchizophreniaSOPRegulatory affairsRespiratoryoncoRheumatologySafety concerns (such as therapeutic ratio with respect to possible adverse effects)Screen patientsThoracic surgeryVaccinesValidationVerification Medical devices NegotiationAllergy and immunologyAntibodiesBiomarkersBiopharmaceuticalsCancerCardiologyCardiovascular diseasesClinical monitoringClinical DevelopmentClinical operationsClinical pharmacologyClinical researchClinical Study DesignClinical trial audits and inspectionsClinical trial budgetingClinical trial designClinical trial managementClinical trialsCTMSData entryData ManagementDrug development processDrug regulatory authoritiesDrug Safety and PharmacovigilanceDrug safety assessmentEfficacy trialsElectronic Data Capture (EDC) Emergency medicineEndocrinologyEnglishEthics submission and approval process

Skills and Expertise

BrightOwl Assessment :
Analyze dataEthics committee submissionsInteract with CROsInteract with ethics committeeLiaise with research teamlifescience Monitor a clinical studyNetwork Report dataSolve problemsSchedule trial visitsCollaborate with principal investigatorCommunicate with investigator Control dataConduct site initiation Monitor a clinical studyNegotiation Monitor a clinical studyClinical data collectionCreate clinical documentsCommunicate with sponsorCoordinate with the ethics commitee Control data Interact with nurses Interact with physicians Interpret data Analyze dataCollaborate with project teamNegotiate budget Creates a collaborative team environment
Self Assessment :
Monitor a clinical studyMonitor clinical trials Monitor dataMonitoring enrolmentMonitoring subject complianceNegotiate budget Negotiate payment schedulesNegotiate protocol details NegotiationNew indications of marketed drugOperate research equipmentOral presentationPatient liaisonPatient recruitmentPre-study procedures Provide study site fileProvide trainingRegulatory documentationRegulatory submissionsReport dataReport non-compliance incidentsReport serious adverse events (SAE)Research at universitiesResolves queriesRetrieve study documentsReview data interpretationReview exclusion criteriaReview inclusion criteriaReview medical reportsSchedule sponsor monitoring visitsReview vendor reportsSchedule trial visitsScheduling trial visitsScreen patientsSerious Adverse Event (SAE) ReconciliationSet up a clinical studySetup of research equipmentShipment of biological specimenSolve problemsSpecimen processingVerify dataWork under specific instructions Act as the main line of communication between the sponsor and the investigator CTMS Interact with nurses Interact with physicians Interpret data Search literature on clinical trials Report dataAdministrative supportAdverse event reportingAdvise on medical perspectivesAlzheimerAnalyze dataApprove queriesArchive documentationArchive study documentsAssess adverse reactionsAssess site feasibilityAssess subject safetyAssist study siteAssist with proceduresAssist with routine testsAttend investigator meetingCapture data on source documentsClinical data collectionCoachCoach staffCollaborate with medical teamCollaborate with principal investigatorCollaborate with project teamCollect patient forms and questionnairesCommunicate with investigatorCommunicate with sponsor Monitor a clinical studyComplete case report form (CRF)Complete study proceduresConduct monitor visitsConduct research at universitiesConduct site initiationConduct post-marketing surveillance studyConduct the trialConduct university research Confirm protocol complianceContact potential subjectsContract approvalControl dataControl protocol versionsCoordinate with the ethics commiteecoordinating research projectsCreate clinical documentsCreate study documentsCreates a collaborative team environmentCTMSData codingData entryData miningData validationData verificationData analysisDiscuss treatments with investigatorDistribute study documentsDistribute trial suppliesDocument adverse eventsEnsure data consistencyEnsure data integrityEnsure good clinical practice (GCP)Estimate subject complianceEthics committee applicationEthics committee submissionsFinancial administrationGastrointestinal diseasesGuide staffHandle callsInformed consent processInitiation visitInteract with CROsInteract with ethics committeeInteract with nursesInteract with pharmacistsInteract with physiciansInterpret dataLiaise with doctorsLiaise with research teamLogging enrolmentMaintain clinical evaluation reportsManage clinical trial files/documentsManage Clinical Trial Management System (CTMS)

Area / Region

Ghent, Belgium

Others

Driving License
  • Yes

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