Luca brings over 20 years of experience in Operations and Supply Chain Management in 2 major multinational USA based corporations in the Consumer and Pharma business.
In these roles, he managed positions of increasing responsibility in Engineering, Maintenance, Production, Logistics, IT, Operations and General Management.
Today, he’s leading the Janssen Clinical Supply Chain organization and is responsible for all activities required to plan, source, make and distribute clinical supplies for all on-going clinical trials at Janssen.
Luca holds a Master of Science degree in Mechanical Engineering from the University of Rome Tor Vergata in Italy. In addition to this, he holds Six Sigma, Lean and APICS certifications.
Three University degrees at the University of Augsburg
5 years of Supply Chain Management responsibilities in automotive electronics industry
12 years of Management responsibilities in multiple roles (SCM, IT, Sales) in the pharma industry
Since 2014 Head of Clinical Trial Supply (Sales) of Teva Europe. Offering Teva widest pipeline of pharmaceuticals, placebos and manufacturing for clinical trial purposes.
Since 2017 Head of Global Health Tendering of Teva Global. Offering Teva widest pipeline to NGOs, GOs and UN related organizations.
Married and father of three beautiful kids
Vanessa is the MD of Clinical Services International (CSI) a leading provider of Clinical Trial Supplies to the Biopharmaceutical Industry.
Vanessa started her career as a research associate at Scotland Yard. Subsequently she worked for leading CROs and with some of the largest biopharmaceutical and Biotechscompanies to provide innovative solutions.
She has extensive experience in drug development from Preclinical to registration and commercialization strategies and has secured product registration for several orphans and first in class drugs.
She has a PhD in Cardiovascular Genetics from UCL, an MBA from Cambridge and Masters in Market Access from University m University of Lyon.
At MSD from 2012 and before worked with comparator sourcing since 2004 at a few wholesalers and a CMO. Started career in product management of medical devices and OTC products. M.Sc. in Engineering in 1995 and proficient in English, German, Italian and Swedish.
Passionate about clinical trial supply chain and clinical trials in general, Bernard started in a Phase I Clinic, developing analytical methods and combining both his Chemistry & Pharmaceutical degrees. After that it was 25 years of anything touching clinical trial supply chain: starting in an IRT department, then moving to a manufacturing environment, followed by outsourcing, heading a global clinical supplies unit of a Big Pharma company, 2 years as QA, and finally started 14 years ago at PPD, now part of Thermo Fisher Scientific. At PPD, part of Thermo Fisher Scientific, Bernard started on the operational side, but is now on the support side, ensuring the department is ready for growth, from an improvement, compliance & resource perspective
