Azzurra Mutti
Clinical Research Associate at mectron- Claim this Profile
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Italiano Native or bilingual proficiency
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Inglese Professional working proficiency
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Francese Elementary proficiency
Topline Score
Bio
Experience
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Mectron Dental
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Italy
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Medical Device
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1 - 100 Employee
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Clinical Research Associate
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Dec 2019 - Present
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greenteg AG
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Switzerland
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Appliances, Electrical, and Electronics Manufacturing
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1 - 100 Employee
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Clinical Study Coordinator
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May 2019 - Oct 2019
• Plan, coordinate, and control external studies and scientific projects • Plan, coordinate, and conduct internal studies • Write and review study protocol, collect and maintain research study data, monitor and report adverse reaction • Managing documents for Ethics approval and consecutive fulfilment of duties • Facilitator to coordinating study team members • Drawing up Case Report Forms, database design and all study documentation • Coordinator Center activities (managing the supporting documents for Ethics Committee, site monitoring, quality assurance of data processing) • SOP writing Show less
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IOR Institute of Oncology Research
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Bellinzona, Canton Ticino, Svizzera
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Assistant Research Scientist
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Feb 2018 - Mar 2019
• Screening/Identification of small molecule targeting FOXA1 activity in prostate cancer • Screening/Identification of small molecule targeting SPOP activity in prostate cancer • Responsible to design and implement experiments for drug screenings projects • Screening/Identification of small molecule targeting FOXA1 activity in prostate cancer • Screening/Identification of small molecule targeting SPOP activity in prostate cancer • Responsible to design and implement experiments for drug screenings projects
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Missione CRA
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Italy
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Higher Education
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Clinical research Course
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Sep 2018 - Nov 2018
Topics: • Methodology and Regulation of clinical trials; • Good Clinical Practice (ICH-GCP); • Standards for Good Manufacturing Practice (GMP); • Pharmacovigilance; • Quality Systems and Quality Assurance (QA); Tasks of Monitors referred to paragraph 5.18 of Annex 1 to the Ministerial Decree July 15, 1997 (including Pre-Study Visit, Site Initiation Visit, Site Monitoring Visit and Close Out Visit); • Regulation (EU) N° 536/2014-Chapter I and II; • Workshop on Site Selection, Pre-Study Visit, Essential Documents, Drug Accountability. Show less
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IOR Institute of Oncology Research
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Bellinzona
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Master Thesis Student
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Sep 2016 - Aug 2017
• Screening/Identification of small molecule targeting ERG activity in prostate cancer • Responsible to design and implement experiments for drug screenings projects • Screening/Identification of small molecule targeting ERG activity in prostate cancer • Responsible to design and implement experiments for drug screenings projects
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Ente Ospedaliero Cantonale (EOC)
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Switzerland
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Hospitals and Health Care
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700 & Above Employee
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ICH GCP
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Jun 2017 - Jun 2017
ICH GCP course - Investigator LevelThis course has been recognized by Swissethics
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ICH GCP secondo livello
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Jun 2017 - Jun 2017
GCP Sponsor-Investigator LevelThis course has been recognized by Swissethics
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University of Pisa
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Pisa, Italia
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Trainee
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Jan 2013 - Sep 2013
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Pepe rosso
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Manhattan. NYC
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Cameriera
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Jun 2009 - Oct 2009
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Cacio e pepe
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Manhattan, NYC
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Cameriera
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Jun 2008 - Oct 2008
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Education
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Università di Pisa
Bachelor's degree, Scienze biologiche e biomediche -
Literacy partners
Enghish Course -
City University of New York-Hunter College
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Università di Pisa
Master's degree, Biology Applied to Biomedicine -
TRAINING AND RESOURCES IN RESEARCH ETHICS EVALUATION
Introduction to Research Ethics