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Summary

i’m currently finishing a phd at the University Hospital of antwerp (uza) and University of antwerp in which i was responsible for the management and execution of (pre)Clinical experiments. i was constantly working into a clean-room area strictly regulated by cGMP guidelines, also for Pharmaceuticals production. during this period, i was able to acquire deep experience in case Report Writing, sops, etc., cGMP and other relevant regulatory guidelines, in addition to a strong organizational, analytical, management, and operational mindset.

being also able to fluently relate with people belonging to different r&d departments for successful completion of Research studies.
previously i was part for several years of a Pharmaceutical firm called acom s.p.a. in which i was taking care of Report Writing, sops, batch-record tracking, as well as Pharmaceuticals production (always working into a clean-room area regulated by cGMP guidelines).

i graduated in industrial Pharmacy, being able to get knowledge and overview of eu regulations about Pharmaceuticals and development of medical products in general.

Experiences

Current Experience

  • Member of the Editorial Board


    Since January 2016

    Member of the editorial board at the italian association of nuclear Medicine and Molecular Imaging (aimn)

    Member of the Editorial Board at the Italian Association of Nuclear Medicine and Molecular Imaging (AIMN)

  • Postgraduate Researcher

    Antwerp, Belgium
    Since March 2014

    project title: "development of [18f]poly(2-oxazoline)-duramycin and [18f]poly(2-oxazoline)-rgd as radiotracers for In Vivo imaging of tumor environment"

     

    ·       Planning, management, and follow-up of (pre)Clinical studies

    ·       studies record tracking

    ·       write protocols (sops, etc.)

    ·       write reports

    ·       Research in oncology

    ·       Scientific writing and oral Communication

    ·       working in clean-room environments (GMP)

    ·       xenografts tumor models

    ·       in-vitro and in-vivo experiments

    ·       animal handling

    ·       qc of radiopharmaceuticals (HPLC, gc,…)

    ·       Molecular Imaging (spect-ct, pet-ct)

    ·       radiopharmacy

    ·       Statistical Analysis

     

     

     

    Project title: "Development of [18F]poly(2-oxazoline)-duramycin and [18F]poly(2-oxazoline)-RGD as radiotracers for in vivo imaging of tumor environment"

     

    ·       Planning, management, and follow-up of (pre)clinical studies

    ·       Studies record tracking

    ·       Write protocols (SOPs, etc.)

    ·       Write reports

    ·       Research in oncology

    ·       Scientific writing and oral communication

    ·       Working in clean-room environments (GMP)

    ·       Xenografts tumor models

    ·       In-vitro and in-vivo experiments

    ·       Animal handling

    ·       QC of radiopharmaceuticals (HPLC, GC,…)

    ·       Molecular imaging (SPECT-CT, PET-CT)

    ·       Radiopharmacy

    ·       Statistical analysis

     

     

     

  • Postgraduate Researcher

    Antwerp, Belgium
    Since March 2014

    project title: "development of [18f]poly(2-oxazoline)-duramycin and [18f]poly(2-oxazoline)-rgd as radiotracers for In Vivo imaging of tumor environment"

     

    ·       Planning, management, and follow-up of (pre)Clinical studies

    ·       studies record tracking

    ·       write protocols (sops, etc.)

    ·       write reports

    ·       Research in oncology

    ·       Scientific writing and oral Communication

    ·       working in clean-room environments (GMP)

    ·       xenografts tumor models

    ·       in-vitro and in-vivo experiments

    ·       animal handling

    ·       qc of radiopharmaceuticals (HPLC, gc,…)

    ·       Molecular Imaging (spect-ct, pet-ct)

    ·       radiopharmacy

    ·       Statistical Analysis

    Project title: "Development of [18F]poly(2-oxazoline)-duramycin and [18F]poly(2-oxazoline)-RGD as radiotracers for in vivo imaging of tumor environment"

     

    ·       Planning, management, and follow-up of (pre)clinical studies

    ·       Studies record tracking

    ·       Write protocols (SOPs, etc.)

    ·       Write reports

    ·       Research in oncology

    ·       Scientific writing and oral communication

    ·       Working in clean-room environments (GMP)

    ·       Xenografts tumor models

    ·       In-vitro and in-vivo experiments

    ·       Animal handling

    ·       QC of radiopharmaceuticals (HPLC, GC,…)

    ·       Molecular imaging (SPECT-CT, PET-CT)

    ·       Radiopharmacy

    ·       Statistical analysis

Past Experience

  • Production worker Montecosaro Scalo, Province of Macerata, Italy

    April 2009 --- November 2013

    production of [18f]fdg

     

    ·       work according to gpm guidelines

    ·       GMP guidelines adoption

    ·       batch record tracking

    ·       regulatory processes

    ·       write reports

    ·       radiopharmaceuticals production for Clinical use

    ·       working in clean-room environments (GMP)

    ·       qc of radiopharmaceuticals

  • Pharmacist Porto San Giorgio, Province of Fermo, Italy

    September 2010 --- April 2011

    ·       identify and solve medication related problems

    ·       Pharmaceutical legislation

    ·       evaluate and document Clinical responses

    ·       consult with team members and physicians 

    ·       provide appropriate medication information

    ·       Customer Service and counseling

    ·       Clinical Applications

    ·       Inventory Management and control

    ·       medication safety

    ·       knowledge of medication and cross- interactions

    ·       Pharmaceutical compounding

  • Intern Montecosaro Scalo, Province of Macerata, Italy

    November 2009 --- May 2010

    project title: "sarar synthesis for 64-copper coordination"

     

     

    ·       radiopharmacy

    ·       develop Research project

    ·       Medicinal Chemistry

  • Research internship Knoxville, TN, United States

    May 2009 --- July 2009

    the University of tennessee medical center (utmc), usa

    department of radiology

     

    the University of tennessee of knoxville (utk), usa

    department of chemistry

     

    project title: "no-carrier-added radiohalogenations utilizing organoboranes: the synthesis of i-123-labeled curcumin"

     

    ·       radiopharmacy

    ·       Molecular Imaging

    ·       alzheimer Research

    ·       Medicinal Chemistry

Personality

Self Assessment :
AdaptabilityAnalytical thinkingApproachabilityAttention to detailAuthenticityCollaborationCommunicativeCompetitivenessCoordinationCreative thinkingCritical thinkingCuriosityDiligenceEfficiencyIndependenceInnovative thinkingInterest in knowledgeKindnessOptimismOrganizationOrientationPerspectiveProactivityProblem solvingResponsibilitySelf-disciplineSelf-confidenceTrustSociabilityStrategic thinkingService orientedResiliencyResult OrientedFlexibility

Knowledge

Self Assessment :
Animal models Biochemistry Labtechnician Negotiation Lab scale batches R&D Scientific writingAnalysisAnalytical ChemistryAnalytical methodsAnalytical proceduresAnalytical techniquesAngiogenesisAnimal ModelsAnimal trialAseptic ProcessingAseptic TechniquesBioanalysisBiomarkersBiomedical SciencesCancerCancer ResearchCell Based AssaysCell CulturecGMPCharacterizationChemistryChromatographyCleanroomCommunication SkillsComplianceCompliance with regulationsContinuous ImprovementCurrent Good Manufacturing Practice (CGMP)Data AnalysisData ScienceDiagnostic radiologyDiagnosticsDiagnostic marketDrug DeliveryDrug DevelopmentDrug development processElectronicsEnglishEnglishEthics submission and approval processExperimentationGalenicsgas chromatographyGMPGood Laboratory Practice (GLP)Good Manufacturing Practice (GMP)GraphPad PrismHardware DiagnosticsHealthcareHealthcare industryHistologyHospitalsHPLCImmunohistochemistryImmunohistochemistry (IHC)In VitroIn VivoInformaticsIsotope SynthesisKnowledge of the drug development processLaboratoryLaboratory Animal MedicineLaboratory ManagementLaboratory ResearchLaboratory SkillsLaboratory TechniquesLaboratory testingLabtechnicianLeadershipLife SciencesLifesciencesLiquid Chromatography-UV (LC-UV)Liquid chromatographyMedical ImagingMicrosoft ExcelMicrosoft OfficeMicrosoft PowerpointMicrosoft WordMolecular DiagnosticsMultilingualNanomedicineNanotechnologyNegotiationNuclear radiology oncoOncologoncologyOrganic ChemistryOutlookPharmaceutical DevelopmentPharmaceutical IndustryPharmaceutical ManufacturingPharmaceutical ResearchPharmaceutical SciencesPharmaceuticalsPharmaceuticsPharmacistsPharmacokineticsPharmacyPowerPointPre-clinical researchPreclinical developmentPreclinical regulations and practicesPreclinical ResearchPreclinical SafetyPresentation SkillsPresentationsProblem SolvingProblem-solving methods and troubleshootingProgrammingPurificationQA complianceQC releaseQuality AssuranceQuality Assurance (QA)Quality Control (QC)Radiation oncologyRadiologyRandomization and blindingRandomization SystemsRegulatory affairsReport WritingResearchscienceScientific CommunicationsScientific WritingSDS-PAGESmall moleculesSocial MediaSocial Media MarketingSocial SkillsSoftware DocumentationStability testsStandard Operating Procedure (SOP)StatisticsTeam BuildingTeam LeadershipTeam ManagementTeamworkTrainingTroubleshootingValidationVerificationWriting Study Procedures and SOPs
LinkedIn Assessment :
Pharmaceutical IndustryChemistryscienceTeamworkComputer ScienceRadiochemistryAnalytical ChemistryGMPInternet ServicesNuclear ChemistryChimicaMedicinal ChemistryScienze naturaliEnglishChimica farmaceuticaOrganic ChemistryBiologia molecolareRicercaResearchPharmacyspanishInorganic ChemistryQuality AssuranceLife SciencesBiotecnologColtura cellulareFarmaceuticaLingua ingleseHPLCmolecular biologyChimica analiticaIndustria FarmacNorme di buona fabbricazioneScienzaIn VitroSecondary EducationIn VivoMolecular ImagingRadioligand BindingRadioimmunoassayBinding AssaysMedical ImagingPMODCell CultureImmunohistochemistrySmall Animal ImagingCancer ResearchBiotechnologyPharmaceuticsSOP

Skills and Expertise

Self Assessment :
Analytical skills Analyze data Assure medical quality Create SOPs Control data Guide students Interact with nurses Interact with physicians Interpret data Molecular Diagnostics Report data Write papers Write protocolsAdjust methodsAdjust processes Adjust processes and methodsAnswer, transfer and handle incoming calls as needed.Aseptic processingAseptic techniquesAssist with experimentsAssist with proceduresAssist with routine testsAssist with site trainingAttend seminarsAttend seminars, courses and meetings within and outside the companyBiomarker Researchbudgeting of R&D activitiesCell cultureCoachCoach staffcollaborate in research projects at universitiesCollaborate with principal investigatorCollaborate with project teamCollect dataCommunicate with investigatorCommunicationConduct animal studiesConduct limited data and/or statistical analysis.Conduct literature searchesConduct literature searches.Conduct maintenance visitsConduct research at universitiesConduct studiesConduct university research Create SOPsCreate standard operating procedure (SOP)Design IT solutionsDesign scientific experimentsDesign studiesDesign studyDesign the studyDevelop protocolsDevelop study budgetDirect co-workersDirect co-workers to achieve resultEnsure good clinical practice (GCP)Ethics committee applicationEthics committee submissionsEvaluate protocolsExecute internal/external quality assurance assessmentsExecute scientific projectsFollow-up of external auditsFollow-up of internal auditsFollow up training programsFollow up projectsFollow-up of quality assurance activitiesGeneral office managementGuide studentsHandle callsHandle incidentsInteract with ethics committeeInteract with nursesInteract with pharmacistsInteract with physiciansInteract with pre-clinical scientistsInteract with statisticiansInterpret analytical resultsInterpret dataInterpret scientific dataInterpret research resultsLiaise with research teamlifescienceMaintain strong relationshipsMaintenance of biomedical equipmentmanaging a small teamManufacture of GMP batchesManufacture of non-GMP and GMP batchesManufacture of non-GMP batchesManuscript preparationNetworkNon-aseptic processingPlan experimentsPlan work to meet objectives and deadlinesPre-study procedures Prepare final reportPrepare manuscriptPreparing referral lettersPresent data at congressProcure and prepare samplesProvide technical supportProvide trainingPublication of articlesPublish scientific projectsQuality control processQuality testing of Investigational Medicinal Products (IMPs)R&DRead medical literatureRead medical literature to maintain current awareness and knowledgeReferral lettersRegulatory documentationResearch at universitiesReview dataSetup of research equipmentSolve problemsStatistical analysisSupervise techniciansTrain off site staffTrain on site staffTrain StaffUse laboratory techniquesVerify dataWork collaboratively with the other members of the clinical research team Work cross-functionallyWork under specific instructionsValidate dataWrite documentsWrite final reportsWrite papersWritten presentation

Education

  • Master's degree in Industrial Pharmacy from Università di Camerino in 2013
  • High school degree in Science from I.S.T.P.S. Liceo Scientifico "E. Medi" in 2006

Training and Certification

  • Radioprotection course in 2017 Training
  • Duolingo Proficiency Exam in English: Advanced in 2017 Certification
  • EU Scholarship - Android Development for Beginners in 0000 Certification
  • FELASA Cat. C in 0000 Certification

Languages

BrightOwl Assessment:
Self Assessment:
Italian
Native
Spanish
Full Proficiency
English
Full Proficiency
Dutch
Elementary Proficiency

Work Preferences

  • Notice Period:
    3 weeks
  • Positions I am interested in:
    Clinical Research Consultant Compliance Manager Industrial Pharmacist Junior Scientist Lab Analyst Pharmacist Post-doctoral Fellow Postdoctoral fellow Postdoctoral Research Fellow Preclinical Scientist Project Engineer QA Consultant QA Lead QC Specialist QC/QA Manager Qualified Person Quality Assurance (QA) Manager Regulatory Affairs Associate Regulatory Affairs Consultant Scientific consultant Scientific Researcher Scientist Clinical Operations Manager
  • Locations I am interested in:
    Antwerp, Belgium Brussels, Belgium Eindhoven, Netherlands Ghent, Belgium Leuven, Belgium Mechelen, Belgium Vilvoorde, Belgium
  • Work From Home:
    Yes, 0 to 1 days per week
  • International:
    Yes

Publications

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

Area / Region

Antwerp, Belgium

Others

Driving License
  • Yes

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