Raffaele Di Marzo

EU QPPV at Kedrion
Raffaele Di Marzo

Graduated in Medicine and Surgery with more than 25 years of experience in Medical Departments of national and multinational pharmaceutical companies, I have acquired a robust knowledge of Pharmaceutical Medicine in its different fields of application, (R&D, Medical Affairs, Pharmacovigilance, Regulatory Affairs and Quality) also serving as an intermediary between requests of the competent authorities and the needs expressed by all functional areas of the company as well as support for the parent company and to the strategic functions for the maintenance of the business (Marketing, Market Access and Commercial). I have ability to work both independently, with frequent interruptions and changes in priorities and in compliance with predetermined timeframes, or coordinating and managing teams. leadership, communication skills, adaptability, problem solving attitude, a solid scientific background, the fluent use of the English Language and the availability to national and international mobility, complete my profile. Therapeutical Areas in which I have worked/working: Immunology, Vaccines, Pain, Critical Care, Oncology, Neurology, Infectious Diseases, Osteoporosis, Nutraceuticals, Plasma derivatives.

1998-2002: Medical Director, Elan Pharma Italia /Segix Italia S.p.A
2002-2016: Deputy Director Clinical, Epidemiology, Pharmacovigilance/Deputy Director Scientific & Pharmaceutical Affairs Department, Sanofi Pasteur MSD S.p.A

2017 - at present Kedrion S.p.A.:
Head of Pharmacovigilance Department & EUQPPV: overall, responsible for the establishment and maintenance of the Kedrion pharmacovigilance system, responsible for Group Pharmacovigilance Staff (10 FTE), the coordination and organization of the pharmacovigilance activities within the Kedrion Group, setting and implementing global policies, guidelines and standards.

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