Stefano Pozzi

Stefano Pozzi

Associate Director, Clinical Trials | Gct S&O Late Development @ Bristol Myers Squibb

About Stefano Pozzi

Stefano Pozzi is the Associate Director of Clinical Trials at Bristol Myers Squibb in Boudry, Neuchâtel, Switzerland, with extensive experience in managing clinical trials and medical affairs in Hematology, Oncology, Neurology, and Inflammatory Diseases.

Current Role at Bristol Myers Squibb

Stefano Pozzi is the Associate Director for Clinical Trials in the GCT S&O - Late Development division at Bristol Myers Squibb, based in Boudry, Neuchâtel, Switzerland. In this role, he oversees clinical trials, ensuring they adhere to regulatory requirements and company standards.

Previous Positions at Bristol Myers Squibb

Before becoming an Associate Director, Stefano Pozzi served as the Senior Global Trial Manager for GDO/NRDG&ISR at Bristol Myers Squibb from 2019 to 2021. He was responsible for global trial management, overseeing multiple clinical trials simultaneously and ensuring their successful completion.

Experience at Celgene

From 2016 to 2020, Stefano Pozzi held various roles at Celgene in Boudry, Canton of Neuchâtel, Switzerland. He started as Manager of Medical Affairs Operations, a position he held for three years, and then advanced to Senior Manager in Global Medical Affairs, where he worked for one year. In these roles, he contributed significantly to medical affairs operations and global project management.

Early Career at Novartis and Clinika

Stefano Pozzi worked at Novartis from 2011 to 2016 in Italy, first as a CRA Oncology for one year and then as a Study Manager Oncology for four years. Prior to Novartis, he was a Product Specialist & Scientific Manager for Trauma at Clinika S.r.l. from 2010 to 2011. These roles helped him build a solid foundation in oncology research and clinical trial management.

Academic Background

Stefano Pozzi earned his Master's degree in Biology from Università degli Studi di Milano, where he studied from 1997 to 2002, followed by a Ph.D. in Biotechnology from Università degli Studi di Milano-Bicocca, completed between 2007 and 2009. He also held research fellow positions at Università degli Studi di Milano-Bicocca and FONDAZIONE IRCCS ISTITUTO NEUROLOGICO CARLO BESTA, further strengthening his research expertise.

Expertise in Clinical Development and Medical Affairs

Stefano Pozzi has extensive experience in managing clinical trials from Phase I to IV, as well as Non-Interventional Studies (NIS) and Post Approval Safety Studies (PASS). His operational background spans across clinical development and medical affairs in Hematology, Oncology, Neurology, and Inflammatory Diseases. He possesses deep knowledge of Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GVP), making him a valuable asset in the global pharmaceutical environment.

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