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Experiences

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) • 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 science)" rel="nofollow">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

Knowledge

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

Education

  • 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

Others

Driving License
  • Yes

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