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Summary

I've completed a Master in Clinical Research organized by the University of Milan and I’ve also ended my trainee period at the Institute of Pharmacological Research “Mario Negri” in Milan. From this experience i became a real passionate about clinical research and i want to work in this field as soon as possible. I've never worked independently as CRA but i did over 10 visits on-site alongside with senior CRAs. I'm searching a positions as Junior CRA or CTA.


Kind Regards,

Paolo

Experiences

Past Experience

  • Research Trainee Milan, Italy
    January 2015 --- October 2015

    worked on the European Randomized Multicenter Double-Blind trial on Alzheimer’s disease NILVAD alongside with the clinical monitor. My duties were those of a CRA, and i've fullfilled all the requirements of the italian legislations to become a Clinical Monitor myself for the italian law (DM 15/11/2011).

    In addition to that I've followed other two trials on the cardiovascular system: the first was about the prevention of anthracycline cardiotoxicity confronting two different therapy and the other one was about on the best immunosuppressive therapy after an heart transplant.

    I’ve also worked on a Systematic Review on the Alzheimer’s disease with the article that will be published in the first quarter of 2016.

    During this year i’ve also had the opportunity to see how it work an Ethical Committee from the inside because I had the opportunity to take part in several reunions of the Milano Area B Ethical Committee and i’ve also attended several meetings and conferences on Clinical Research.

  • Biologist
    September 2014 --- November 2014

    Worked in the department of Research and Development at the "Istituto Zooprofilattico di Teramo". Worked mainly on parasites and zoonoses using several techniques such us PCR, RT-PCR, electrophoresis and DNA extraction.

Personality

Self Assessment :
AdaptabilityApproachabilityAttention to detailCollaborationCommunicativeCoordinationAuthenticityCritical thinkingOrganizationProactivitySociability

Knowledge

Self Assessment :
Clinical Data ManagementClinical monitoring Cell biologyBiologyBiotechnologyBiopharmaceuticalsClinical pharmacologyDrug Safety and PharmacovigilancePharmaceutical ResearchPharmaceutical SciencesPharmaceuticalsPharmaceutics
LinkedIn Assessment :
Scienze naturaliBiotechnologyPharmaceuticsClinical researchClinical trialsICH-GCPNeuroscienzePCRSperimentazioni clinicheBiotecnologíaRicerca clinicaRicercaIndustria FarmacéuticaMicrosoft ExcelColtura cellularePublic SpeakingMicrosoft Office

Skills and Expertise

Self Assessment :
Clinical data collection Develop clinical trial protocols Monitor a clinical study Search literature on clinical trials

Education

  • Master's degree in Clinical Research from Università degli Studi di Milano in 2015
  • Bachelor's degree in Pharmaceutical Biotechnology from Università degli Studi dell'Aquila in 2014
  • BSc in General Studies - Biotechnology in Biotecnologie from University of Abertay Dundee in 2011

Training and Certification

  • Formazione Generale in tema di Sicurezza sul Lavoro Certification
  • GCP Training Certification

Languages

BrightOwl Assessment:
Self Assessment:
Italian
Native
English
Full Proficiency

Work Preferences

  • Notice Period:
    1 week
  • Positions I am interested in:
    Clinical Research Associate (CRA) Clinical Trial Assistant (CTA) Clinical Data Manager (DM) associate Clinical Project Manager Clinical Trial Specialist (CTS) Regulatory and Start-Up Specialist Study Start-up Specialist
  • Work From Home:
    No
  • Work Regime:
    Permanent position
  • International:
    Yes

Area / Region

Italy

Others

Driving License
  • Yes