Pierre Edern Stoltz
About Pierre Edern Stoltz
Pierre Edern Stoltz is the Associate Director of Clinical Data Management at Bristol Myers Squibb in Boudry, Neuchâtel, Suisse, with over a decade of experience in clinical data management across various companies.
Current Role at Bristol Myers Squibb
Pierre Edern Stoltz currently holds the position of Associate Director, Clinical Data Management at Bristol Myers Squibb in Boudry, Neuchâtel, Suisse. In this role, he oversees clinical data management operations, contributing to the execution and evaluation of clinical trials. His responsibilities likely include managing data collection processes, ensuring data integrity, and collaborating with cross-functional teams to support drug development and regulatory submissions.
Previous Roles at Bristol Myers Squibb
Prior to his current role, Pierre Edern Stoltz served as Senior Manager, Clinical Data Management at Bristol Myers Squibb from 2021 to 2022. During his tenure as Senior Manager, Pierre was responsible for overseeing specific clinical trials, managing clinical data teams, and ensuring the accuracy and quality of clinical data used for regulatory evaluations and submissions. His experience in this position set the stage for his promotion to Associate Director.
Career at Celgene
Pierre Edern Stoltz had a notable career at Celgene where he advanced through several roles related to clinical data management. He served as Manager, Clinical Data Management for six months in 2020-2021. Before that, he was a Senior Clinical Data Manager from 2018 to 2020 and Clinical Data Manager from 2016 to 2018. His experience at Celgene included managing clinical data for drug development processes, ensuring data quality, and collaborating with clinical research teams. These roles contributed to his substantial expertise in clinical data management.
Experience at IQVIA
Before joining Celgene, Pierre Edern Stoltz worked at IQVIA, beginning as an Associate Clinical Data Coordinator in 2013, and progressing through roles including Clinical Data Coordinator, Senior Clinical Data Coordinator, and Associate Data Team Lead until 2016. His roles at IQVIA involved hands-on clinical data tasks, team leadership, and contributing to the data management aspects of clinical trials. His tenure at IQVIA provided a strong foundation for his subsequent roles in the pharmaceutical industry.
Educational Background
Pierre Edern Stoltz completed his Master 2 (M2) in Drug Sciences - Pharmaceutical Conception, Development, and Synthesis at Université d'Auvergne (Clermont-Ferrand I) from 2010 to 2012. This advanced education provided him with in-depth knowledge of pharmaceutical sciences, which he has applied throughout his career. Prior to this, he achieved a Licence in Chemical and Biology from Université de Strasbourg, where he studied from 2007 to 2010. His formal education laid a robust groundwork for his expertise in clinical data management.