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Experiences

Current Experience

  • Clinical Research Associate (CRA)


    Since November 2013

Past Experience

  • Stagista

    January 2013 --- June 2013
    redazione della documentazione relativa la presentazione di protocolli di ricerca al comitato etico; affiancamento visite di monitoraggio; Data entry per crf elettroniche di studi osservazionali e interventistici.

  • Ricercatrice

    March 2011 --- March 2013
    sviluppo di sequenze eparino simili come inibitori dell’enzima eparanasi.

  • Stagista

    February 2008 --- March 2008
    analisi test ELISA

Personality

BrightOwl Assessment :
PerspectiveCuriosityAuthenticityKindnessOrganization
Self Assessment :
Attention to detailCollaborationDiligenceIndependenceOptimismOrganizationOrientationProblem solvingReaction to stressTrust

Knowledge

BrightOwl Assessment :
Clinical monitoringOphthalmologyPhases of clinical development (phase I to IV)Clinical researchData Management
Self Assessment :
DiabetesClinical monitoringClinical study reportsDermatologyGood Clinical Practice (GCP)OphthalmologyPhase IIIPhase IVRespiratorySerious Adverse Event (SAE)Statistics
LinkedIn Assessment :
Microsoft Officechimica dei carboidratitecniche cromatografiche (IEC, EC)analisi cromatografiche ad esclusione molecolare ad alta pressione (HP-GPC)Valutazione di analisi NMR (1H, 13C, HSQC)Valutazione di analisi di spettrometria di massa (HPLC)IngleseMetodologia e normative delle sperimentazioni clinicheFarmacovigilanzaGCPsviluppo, pianificazione e organizzazione di una sperimentazione;elementi di bioeticaelementi di economia sanitariaepidemiologia ed elementi di statistica

Skills and Expertise

BrightOwl Assessment :
Interact with nurses Interact with physicians Interpret dataAdministrative supportCollaborate with project team Monitor a clinical studyEnsure good clinical practice (GCP)lifescience Monitor a clinical studySite managementSolve problems
Self Assessment :
Interact with physicians Interact with nursesCapture data on source documentsCollaborate with medical teamCommunicate with investigatorData verificationEnsure good clinical practice (GCP)Initiation visitInteract with pharmacistsMonitoring subject complianceMonitor clinical trials Verify data

Education

  • Master di primo livello in Ricerca Clinica in from Università degli Studi di Milano in 2013
  • Laurea specialistica in Biotechnology from Università degli Studi di Milano-Bicocca in 2011

Training and Certification

  • Health and safetyin the workplace, Legislative Decree 81/2008) in 2015 Training
  • Medical training and study protocol (Therapeutic area: Metabolism and nutrition disordes, Sponsor specific) in 2015 Training
  • Training for fulfilling DM 15.11.2011 requirements in 2014 Training
  • Training on procedures for issuing investigational product to center and site initiation (Sonsor specific) in 2014 Training
  • Training Writing Monitoring Report (Sponsor Specific) in 2014 Training
  • Training on Protocol (Therapeutic Area: Respiratory Diseases - Sponsor specific) in 2013 Training
  • Course of CRA in 2013 Certification

Languages

BrightOwl Assessment:
Italian
Native
English
Professional Proficiency
Self Assessment:
English
Professional Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Positions I am interested in:
    Clinical Research Associate (CRA) Data Manager
  • Locations I am interested in:
    Italy
  • Work From Home:
    Yes, 0 to 2 days per week
  • Work Regime:
    Permanent position
  • International:
    Yes

Publications

    Expert has 1 publications (Will be avalible with full profile)

Area / Region

Busto Arsizio, Province of Varese, Italy

Others

Driving License
  • Yes

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