Preclinical and clinical drug development: scientific, regulatory and ethical aspects (Postgratuated Master Course)
2015 - 2015
Cambridge English Centre (Caserta)
English language course for IELTS (International English Language Testing System)
2014 - 2015
Second University of Naples (Caserta)
Master's Degree in Pharmacy (Faculty of Pharmaceutical Sciences for Environment and Health)
2008 - 2014
Faculty of Pharmaceutical Sciences for Enviroment and Health, Villanueva de la Cañada (Madrid/Spain)
Erasmus Project
2010 - 2010
Istituto Salesiano Sacro Cuore di Maria (Caserta)
High School Diploma (Liceo Scientifico)
2002 - 2007
Giulia Messina Skills
Sperimentazioni cliniche
Industria farmaceutica
Sviluppo Clinico
Scienze naturali
Regulatory Affairs
Oncologia
Biotecnologia
Farmacologia
Farmacovigilanza
Ricerca clinica
Giulia Messina Summary
Giulia Messina, based in Rome, IT, is currently a Regulatory Affairs Manager at CROlife S.r.l.. Giulia Messina brings experience from previous roles at The Janssen Pharmaceutical Companies of Johnson & Johnson, Abbott Medical S.r.l. and Stryker. Giulia Messina holds a 2015 - 2015 Preclinical and clinical drug development: scientific, regulatory and ethical aspects in Postgratuated Master Course @ Catholic University of the Sacred Heart. With a robust skill set that includes Sperimentazioni cliniche, Industria farmaceutica, Sviluppo Clinico, Scienze naturali, Regulatory Affairs and more. Giulia Messina has 1 emails and 1 mobile phone numbers on RocketReach.
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