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.
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.
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
ResiliencyDependabilityInterest in knowledge
SociabilitySelf-disciplineProblem solvingFlexibilityEfficiencyCuriosityCreative thinkingCharmAttention to detailAnalytical thinking
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)
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
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
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
Medical Doctor in Medicine from VUB in 1987
Training and Certification
Medical Doctor in 1987 Training
ICH-GCP in 2014 Certification