
Benedetta Turriziani
Graduate Student

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About me
Associate Director Tissue Diagnostic | oncology and biomarker | clinical research
Education

Sapienza Università di Roma
-Bachelor of Science - BS BiotechnologyExperimental 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 biotechnologyExperimental thesis: "Role of Metabotropic Glutammate Receptor in increasing chemosensitivity of colorectal cancer stem cells to classical chemoterapic drug.”

University College Dublin
2012 - 2016Doctor of Philosophy - PhD Medical Sciencekey words: breast cancer, personalized medicine, system biology, proteomicsExperimental thesis: “Systematic analysis of the dynamic of HRG pathway in breast cancer”.

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

System Biology Ireland
Apr 2012 - Jun 2016Graduate StudentKey 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 2017Clinical Research Associate TraineeDepartment 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 2017Clinical Research AssociateFiralis 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 - nowDiagnostic Scientist
Licenses & Certifications

Design and Interpretation of Clinical Trials
Coursera Course CertificatesJan 2015
An Introduction to Global Health
Coursera Course CertificatesJan 2015
Languages
- itItalian
- enEnglish
- frFrench
- spSpanish
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