Experience

Mectron Dental

• Italy
• Medical Device
• 1 - 100 Employee

• Clinical Research Associate

  • Dec 2019 - Present



greenteg AG

• Switzerland
• Appliances, Electrical, and Electronics Manufacturing
• 1 - 100 Employee

• Clinical Study Coordinator

  • 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



IOR Institute of Oncology Research

• Bellinzona, Canton Ticino, Svizzera

• Assistant Research Scientist

  • 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



Missione CRA

• Italy
• Higher Education

• Clinical research Course

  • 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



IOR Institute of Oncology Research

• Bellinzona

• Master Thesis Student

  • 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



Ente Ospedaliero Cantonale (EOC)

• Switzerland
• Hospitals and Health Care
• 700 & Above Employee

• ICH GCP

  • Jun 2017 - Jun 2017

  ICH GCP course - Investigator LevelThis course has been recognized by Swissethics

• ICH GCP secondo livello

  • Jun 2017 - Jun 2017

  GCP Sponsor-Investigator LevelThis course has been recognized by Swissethics



University of Pisa

• Pisa, Italia

• Trainee

  • Jan 2013 - Sep 2013



Pepe rosso

• Manhattan. NYC

• Cameriera

  • Jun 2009 - Oct 2009



Cacio e pepe

• Manhattan, NYC

• Cameriera

  • Jun 2008 - Oct 2008