Benedetta Turriziani

Benedetta Turriziani

Graduate Student

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location of Benedetta TurrizianiCambridgeshire, England, United Kingdom

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  • Timeline

  • About me

    Associate Director Tissue Diagnostic | oncology and biomarker | clinical research

  • Education

    • Sapienza Università di Roma

      -
      Bachelor of Science - BS Biotechnology

      Experimental thesis: “Role of Metabotropic Glutammate Receptor in the proliferation and differentiation of cerebellar progenitor.”

    • Sapienza Università di Roma

      -
      Master of Science - MS Medical, cellular and molecular biotechnology

      Experimental thesis: "Role of Metabotropic Glutammate Receptor in increasing chemosensitivity of colorectal cancer stem cells to classical chemoterapic drug.”

    • University College Dublin

      2012 - 2016
      Doctor of Philosophy - PhD Medical Science

      key words: breast cancer, personalized medicine, system biology, proteomicsExperimental thesis: “Systematic analysis of the dynamic of HRG pathway in breast cancer”.

    • University of Montpellier

      2016 - 2017
      Master of Science - MS Clinical trial management and design
  • Experience

    • System Biology Ireland

      Apr 2012 - Jun 2016
      Graduate Student

      Key words: oncology, predictive medicine, network biology, proteomicsOptimization of an immunoprecipitation protocol for protein interactions allowing to reduce time and costs to generate large-scale experimental data set resulting in budget savings and international collaborations Part of the management team of the Q-exactive machine of the System Biology Ireland group, ensuring quality standard and basic operation services, running up to 130 samples per weekCollaboration in the development of a licensed proteomic data analysis software, PRODANManagement of two main projects leading to the establishment of a new published method for proteomics analysis and the validation of a new protein interaction Show less

    • CHU Montpellier

      Sept 2016 - Feb 2017
      Clinical Research Associate Trainee

      Department of Clinical Immunology and Therapy, CHU Montpellier, Pr. Christian Jorgensen, Key words: autoimmune diseases; international studies, phase II/III, observational studies.Management of 7 international clinical trials, ensuring the screening and inclusion of 20+ patients in the studies under my responsibility, collaborate to increase the inclusion rate of an additional study by 25% in order to meet an approaching deadlineProblem solving and costumer facing retrieving data from patients and allowing to reach the inclusion target required by the sponsor for 2 studiesTranslation and review of two documents for peer-review submission and potential publication;Other responsibilities:Mainintaing accurate study documentation, including notifying investigators of pertinent protocol changes;Ensure compliance to ICH-GCP guidelines, SOPs, protocol;Patients recruitment and inclusion, management of visits schedule and patients follow-up; Creation of databases collecting data from all the sample available in the group; Show less

    • FIRALIS S.A.

      Mar 2017 - Sept 2017
      Clinical Research Associate

      Firalis SAS, supervisor Pr. Huseyin Firat, Key words: Biomarkers; predictive medicine; autoimmune diseases; international studies, observational studies.International project coordinator of a predictive medicine study on rheumatoid arthritis. Responsible for the update and reorganization of study documentation and ensuring implementation in patients recruitment by 80%;Selection and profiling of Key Opinion Leader (KOL) and management of scientific discussions by international teleconferences, contributing to open 3 new clinical sites and making contact with new KOL potentially interested in the studyTraining of 15+ clinical professional on Standard Operation Procedures and eCRF data entry;Assisted with the financial management of the lab including travel monitoring, consumable usage, budget tracking and proposing new quality control procedure, leading to 10K in saving Other responsibilities:Design and development of a protocol for a commercial collaboration with an external company;Develop, review and edit 10+ clinical trial related documents, including documents for the training of investigators and nurses; Databases creation with over 9 different projects harmonized by the CDISC system for variable comparisonStudy sites follow-up and monitoring in-site visits to ensure absolute adherence to Good Clinical Practice in accordance with ICH-GCP standards, regulatory requirements and study procedures;Interacting with the R&D team for discussion on laboratory issues and collaborative study feasibility;Responsible for sample kit preparation, shipping and maintenance of study supplies;Management of ISF and TMF;Translation of patents; Show less

    • AstraZeneca

      May 2018 - now
      Diagnostic Scientist
  • Licenses & Certifications

    • Design and Interpretation of Clinical Trials

      Coursera Course Certificates
      Jan 2015
    • An Introduction to Global Health

      Coursera Course Certificates
      Jan 2015