Rino Nascari
About Rino Nascari
Rino Nascari is the Director of Clinical Trial Documents, Submissions, and Disclosure at Bristol-Myers Squibb, with extensive experience in clinical data management and regulatory processes.
Current Role at Bristol-Myers Squibb
Rino Nascari currently works as the Director of Clinical Trial Documents, Submissions, and Disclosure at Bristol-Myers Squibb in Princeton, New Jersey. In this role, Nascari serves as the point of contact for the TransCelerate Common Protocol Template and Common CSR Template. His responsibilities include overseeing the creation, submission, and disclosure of clinical trial documents, ensuring compliance with regulatory standards, and leading initiatives to improve quality and productivity while reducing costs and cycle time.
Previous Roles at GSK
Before joining Bristol-Myers Squibb, Rino Nascari held several leadership positions at GSK in Collegeville, PA. From 2015 to 2017, he worked as the Regulatory Business Operations Lead. From 2013 to 2015, he served as the Director of Quality Framework Management, focusing on enhancing quality frameworks. Prior to this, he worked as Director of Business Design from 2012 to 2013, ensuring alignment with business goals. He was also the Director of Clinical Data Management (CDM) Oncology from 2008 to 2011 and Clinical Data Management Regional Head for Phase 2-4 trials from 2006 to 2008. These roles underscore his extensive experience in clinical data management and regulatory processes.
Professional Experience at Eli Lilly and Company
Rino Nascari's career also includes significant experience at Eli Lilly and Company in Indianapolis, IN. From 2005 to 2006, he worked as a Lean Sigma Black Belt for Global Medical, where he applied Lean Six Sigma methodologies to optimize processes. Prior to this, he served as Manager of Clinical Data Management from 2000 to 2004, where he was responsible for overseeing data management operations for clinical trials. His work at Eli Lilly helped lay the foundation for his expertise in continuous improvement and clinical data management.
Educational Background
Rino Nascari holds a Bachelor of Science degree in Biology from Università degli Studi di Firenze. This educational background laid the groundwork for his career in clinical data management and regulatory operations. His academic training in biology has provided him with a solid foundation in the sciences, complementing his professional expertise in the pharmaceutical and clinical trial sectors.
Expertise and Initiatives
Rino Nascari has demonstrated expertise in therapeutic areas such as Oncology and Diabetes. He is known for leading initiatives aimed at improving quality and productivity while reducing costs and cycle time. His strong background in Lean Six Sigma and Continuous Improvement methodologies has enabled him to drive significant change initiatives and continuous improvement efforts. Nascari is also recognized for creating strong relationships and building capability and trust across teams and functions, underscoring his ability to lead complex projects and foster collaboration.