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Summary

I am a medical doctor with a longstanding clinical experience looking for a position as a CRA, CTA, Medical Advisor or research physician. I had a surgical training but I participated to several clinical studies that I've been carrying out starting with the data collecting over the data analysis up to the presentation of diffirent trials on international congresses.

Experiences

Current Experience

  • medical doctor Bruges, Belgium
    Since July 2012

    I now work as a physician for the Belgian railway company. 

    My job in Bruges allows me to develop my clinical experience. As far as it concerns pharmacology my position here allows me to get familiar with medication adverse events, their treatment, reporting and registration.

Past Experience

  • MD (Medical Doctor) Kortrijk, Belgium
    September 1994 --- September 1995

    MD, participation to clinical evalation that studies local recurrences in breast tumors according to pathological tumor characteristics;

    Data collecting, analysis, statiscal treatment and medical writing

  • medical trainee Frankfurt, Germany
    September 1993 --- August 1994

    participation to clinical studies in oncology. Collecting data and clinical findings, data analysis, statistical work out, medical writing, presentations on local and international congresses

Personality

BrightOwl Assessment :
ResiliencyDependabilityInterest in knowledge
Self Assessment :
SociabilitySelf-disciplineProblem solvingFlexibilityEfficiencyCuriosityCreative thinkingCharmAttention to detailAnalytical thinking

Knowledge

BrightOwl Assessment :
Data AnalysisStatistical Data AnalysisClinical monitoringClinical researchClinical trialsGood Clinical Practice (GCP)Medical writingStandard Operating Procedure (SOP)Writing Study Procedures and SOPsSerious Adverse Event (SAE)Drug safety assessmentDrug Safety and PharmacovigilanceClinical Data Management (CDM)
Self Assessment :
Clinical operations NegotiationColorectal surgeryCommunication SkillsData AnalysisData entry BiostatisticsDiagnostic radiologyDiagnosticsDrug InteractionDrug Safety and PharmacovigilanceDrug safety assessmentClinical trial managementClinical trialsEmergency medicineEnglishGastroenterologyHand surgeryHospitalsICH GCP guidelinesICH-GCPGood Publication Practice (GPP)Medical ImagingMedical DevicesMedical writingNeurosurgeryVascular surgeryOrthopedic surgeryOxidative stressPathologyInterventional RadiologyInterpret systematic reviewsClinical study reportsOperating RoomPatient Follow UpSerious Adverse Event (SAE)Search literature on clinical trials Cell biology Animal models Medical devices Scientific writingBiomarkersCancerCardiovascular diseasesCardiologyClinical Data Management (CDM)Clinical monitoring DiabetesClinical researchClinical pharmacology

Skills and Expertise

BrightOwl Assessment :
Monitor a clinical studyClinical data collectionPresent clinical resultsReview clinical study reportsSearch literature on clinical trialsWrite clinical evaluation reportsSerious Adverse Event (SAE) ReconciliationReport serious adverse events (SAE)Advise on medical perspectives Create SOPs Interpret data Report dataAdverse event reportingAssess adverse reactionsAttend seminarsCollect dataConduct literature searchesOral presentationPresent data at congressProvide medical insightsRead medical literatureRead medical literature to maintain current awareness and knowledge Report dataReview medical reportsStatistical analysisUnderstand protocolsWrite combined statistical and medical reportsWrite medical reportsWrite statistical reports Write protocolsWritten presentation
Self Assessment :
Report serious adverse events (SAE)Review study protocolsStudy-related documentsTranslate clinical research concepts into specific objectivesVerify dataWork under specific instructionswrite and maintain clinical evaluation reportsWrite clinical evaluation reportsWrite combined statistical and medical reportsWrite protocolsSupervise clinical monitorsContact potential subjectsApprove queriesApprove patient informationArchive documentation Receptor Pharmacology Analyze dataInteract with CROsManuscript preparation and reviewWrite papersWrite medical reportsWritten presentation Search literature on clinical trials Molecular Diagnostics Interpret data Interact with nurses Assure medical quality Interact with physicians Develop clinical trial protocols Design case record forms Monitor a clinical study Report dataApprove drug supply Approve consent documentsAssist with experiments Use a confocal microscopyAdvise on medical perspectivesAdverse event reporting Write papers Create SOPs

Education

  • Medical Doctor in Medicine from VUB in 1987

Training and Certification

  • Medical Doctor in 1987 Training
  • ICH-GCP in 2014 Certification

Languages

BrightOwl Assessment:
Self Assessment:
Dutch
Native
French
Full Proficiency
English
Professional Proficiency
German
Professional Proficiency

Work Preferences

  • Notice Period:
    12 weeks
  • Positions I am interested in:
    Clinical Research Associate (CRA) Drug Safety Officer Clinical Research Physician Medical Writer Clinical Trial Assistant (CTA)
  • Work From Home:
    No
  • Work Regime:
    Permanent position
    BrightOwl freelancer :    24 Hours per week
    BrightOwl employee
  • International:
    Yes

Area / Region

Londerzeel, België

Others

Driving License
  • Yes