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Current Experience

  • Senior Clinical Research Associate
    Since August 2014
    • Schedules and reviews trial tasks, provides leadership in the delivery of services to clients, ensures that staff fulfill their responsibilities in accordance with policies, procedures, and SOPs. • Serves as a Preceptor for new CRAs • Functions independently with minimal oversight required • May serve as subject matter expert for CTM on monitoring related activities • Monitoring of studies Oncology (Multiple Myeloma; Lymphocytic Lymphoma or Follicular, Breast Cancer)

Past Experience

  • Clinical Research Associate 2
    January 2013 --- August 2014

    Monitoring of studies diabetes Monitoring of epileptic studies Monitoring of psoriasis studies Partecipation Investigator & Monitor Meeting Monitor and maintain ICH-GCP compliance Perform site facilities inspection Conduct on-site study-specific training Perform on site visits in accordance with the monitoring plan Responsible for the completeness and quality of the on-site files Establish site recruitment plan in collaboration with site during Qualification Visit; follow-up and update at Initiation Visit and Monitoring Visit

  • Clinical Research Associate (CRA)
    March 2010 --- December 2012
    - Preparation of document for submission EC (Ethical Committee) and AC Competent Authority - Monitoring authorization procedures - Monitoring Visit, recruitment, implementation of protocol, handling drug and site closing - Coordination of CRO (Contract Research Organization) - Quality Control for CROs and Auditing activities - Updates of AstraZeneca program informatics - Monitoring of studies Oncology - Monitoring of studies Respiratory - Monitoring of studies Cardiovascular - Partecipation Monitors Meeting - Partecipation Investigator Meeting

  • Stage CTA
    September 2009 --- February 2010
    CTA (Clinical Trial Assistant), supporting Pharmacovigilance Unit and Documentation Unit


LinkedIn Assessment :
Clinical trialsClinical monitoringCROICH-GCPCTMSGCPClinical DevelopmentoncologyPharmaceutical IndustryEDCTherapeutic AreasClinical researchOncologProtocolloSperimentazioni clinicheIndustria FarmacBuona pratica clinicaRicerca clinicaSOPFarmacovigilanzaDiabeteSviluppo clinicoMonitoraggio clinicoCattura di dati elettronici


  • Executive MBA in School of Management from MIP-Politecnico Di Milano in 2017
  • Master “Ricerca e sviluppo preclinico e clinico dei farmaci” in Pharmaceutical Medicine from Università degli Studi di Milano-Bicocca in 2010
  • Degree in Science of Biology in Functional and molecular biology from Università degli Studi di Milano-Bicocca in 2009
  • Bachelor degree in Science of Biology in Molecular biology from Università degli studi di Milano - Bicocca in 2006

Area / Region

Sesto San Giovanni, Metropolitan City of Milan, Italy


Driving License
  • Yes