BrightOwl Loader Loading


Current Experience

  • Clinical Research Associate (CRA)
    Since April 2015
    Site opening visits, monitoring visits and closeout visits; Verification of informed consent and Investigator files; verification of CRF and original documents (SDV); Clinical site support: phone contacts, email contact, follow-up letters; Violations of the Protocol, report deviations to the protocol Monitoring of electronic CRF (if applicable); monitoring reports, support for adverse event reporting; support to researchers in the preparation of reports to the Ethics Committees Study progress reports and compliance metrics.

Past Experience

  • Clinical Research Associate Trainee
    October 2014 --- March 2015
    Obtained Certified as CRA according to Italian D.M. 15th November 2011.

  • Pharmacist
    December 2013 --- September 2014
    Worked , with a large team of pharmacists, as galenic drugs preparer and as pharmacist.

  • Pharmacist trainee
    June 2012 --- March 2013
    Educational training program.


LinkedIn Assessment :
sciencemolecular biologyResearchLifesciencesCell biologyBiochemistryCell CultureStatisticsWestern BlottingBiotechnologyLaTeXClinical researchBiochimicaICH-GCPSperimentazioni clinicheIndustria FarmacFarmacologiaFarmacistiRegulatory affairsMicrosoft OfficeSviluppo clinicoBuona pratica clinicaFarmaciaRicerca clinicaRicerca


  • Master degree in Ethical, regulatory and methodological aspects in clinical trials from Università di Roma Tor Vergata in 2014
  • Degree in pharmacy from Sapienza Università di Roma in 2013
  • Scientific high school diploma in from i.t.a.s. Colomba Antonietti di Roma in 2008
  • Qualification to the pharmacist profession in from Sapienza Università di Roma in 0

Training and Certification

  • ECDL Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Area / Region

Rome, Italy


Driving License
  • Yes