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Summary

social skills and competences excellent Communication Skills acquired: five years as Director of a summer camp for children; ten years of theater workshops with four of Teaching. good ability to adapt myself to particular environments thank to my previous work Training in various Hospital situations. organisational skills and competences sense of organization and experience in Project Management in five years to coordinate summer camp for children. computer skills and competences good knowledge of computers in general, Windows, macintosh, ms office, Photoshop, video Editing programs, siebel and SAP. artistic skills and competences music, singing, acting, diction, design, art history. objectives find professional position dynamic, young, providing opportunities for growth and travel. specialties: interpersonal relationships and ability of Nursing.

Experiences

Current Experience

  • Clinical Research Associate Trainee


    Since February 2015
    internship in Clinical research at gmo oncology medical department. main activities perfomed: - visit at site (feasibility, site selection, site initiation, monitoring, remote monitoring, close-out), source data verfication, drug accountability, revision of Investigator folder, reconciliation of Adverse Events, meeting site staff and pricipal Investigator, - trial start up unit (preparation of documents for submission to irb - iec, interface with regolatory affairs), - participation at study science)" rel="nofollow">Protocol and disease Training - checking and revision of trial master file - data managment and data cross-checking - partecipation at project meeting and medical forum with different company profile - partecipation at Investigator meeting - preparation of tools for CRA and slide kit for site staff. Internship in Clinical Research at GMO Oncology Medical Department. Main activities perfomed: - visit at site (Feasibility, Site Selection, Site Initiation, Monitoring, Remote Monitoring, Close-Out), Source Data Verfication, Drug Accountability, revision of Investigator Folder, reconciliation of adverse events, meeting site staff and Pricipal Investigator, - Trial Start Up Unit (preparation of documents for submission to IRB - IEC, interface with Regolatory Affairs), - Participation at study protocol and disease training - Checking and revision of Trial Master File - Data Managment and data cross-checking - Partecipation at project meeting and medical forum with different company profile - Partecipation at Investigator Meeting - Preparation of tools for Cra and slide kit for site staff.

Past Experience

  • Occupational Health Nurse

    February 2012 --- November 2014
    presidium first aid rooms. organization of Health Care based on needs of the occupational physicians regarding the occupational Medicine. performing health checks: blood collection, drug-Testing, spirometry, visiotest, ecg.

  • Employee Customer Care

    May 2011 --- January 2013
    worker front-line customer support Energy industry committed edison. Problem Solving, management practices, claims and customer information.

  • Employee Customer Care

    November 2010 --- June 2011
    Employee customer support italian “yellow pages”.

  • Sales Promoter

    April 2008 --- November 2010
    promoter of personal computers, printers and high-tech products for hp.

Personality

Self Assessment :
Analytical thinkingAttention to detailCollaborationCuriosityAdaptabilityResult OrientedOptimismOrganization

Knowledge

LinkedIn Assessment :
NursingICH-GCPHealth EducationOccupational Health NursingMedical EducationClinical EducationHealthcareMicrosoft OfficeInternetWindowsInternet ExplorerPublic RelationsProblem SolvingCustomer RelationsTeamworkItalianEnglishEnglish GrammarMedical TranslationEnglish TranslationClinical pharmacologyMicrosoft ExcelPublic SpeakingMicrosoft WordComunicazioneRicerca clinicaPowerPointLingua ingleseAssistenza clientiCustomer ServiceClinical research

Skills and Expertise

Self Assessment :
Interact with nurses Interact with physicians Monitor a clinical studyAssist study site Analyze data Build and manage the Trial Master File (TMF)Written presentationVerify dataTrain on site staff Search literature on clinical trials

Education

  • Postgraduate Course in Clinical Research Associate from Università degli Studi di Firenze in 2015
  • Bachelor's Degree in Nursing in Degree in Nursing certified professional Nurse. from Università degli Studi di Torino in 2011
  • Scientific High School Experimental P.N.I. in Traditional Italian Scientific High School but with a thorough study of applied mathematics. from Liceo Scientifico "A. Volta" in 2007

Training and Certification

  • CRA Certification in 2015 Certification
  • BLS-D Executor in 2014 Certification
  • PTC-IRC in 2012 Certification

Languages

BrightOwl Assessment:
Self Assessment:
English
Professional Proficiency
Italian
Native

Work Preferences

  • Notice Period:
    2 weeks
  • Positions I am interested in:
    Clinical Research Nurse Clinical Research Associate (CRA) Clinical Research Coordinator Registered Nurse
  • Locations I am interested in:
    City of London, London, United Kingdom Milan, Metropolitan City of Milan, Italy
  • Work From Home:
    Yes, 2 to 3 days per week
  • Work Regime:
    Permanent position
    BrightOwl employee
  • International:
    Yes

Area / Region

Milan, Metropolitan City of Milan, Italy

Others

Driving License
  • Yes

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