Manuela Preda
About Manuela Preda
Manuela Preda is the Director of Patient Safety at Bristol Myers Squibb in München, Bayern, Deutschland, with over 20 years of experience in the pharmaceutical industry focusing on drug safety and risk management.
Current Role at Bristol Myers Squibb
Manuela Preda currently serves as the Director of Patient Safety at Bristol Myers Squibb in München, Bayern, Deutschland. In this role, she is responsible for overseeing patient safety operations, ensuring compliance with regulatory requirements, and managing risk assessment activities.
Career at Celgene
Manuela Preda held several key positions at Celgene, advancing from Sr. Drug Safety Manager to Director Drug Safety and Medical Information. She worked as an Associate Director Drug Safety and Medical Information from 2015 to 2018, after serving as Sr. Manager Drug Safety and Medical Information from 2014 to 2015. Prior to these roles, she was a Sr. Drug Safety Manager and Drug Safety Manager for Celgene in Munich. Her career at Celgene spanned from 2010 to 2018, demonstrating her growth within the company.
Previous Experience at Kendle GmbH
Before her tenure at Celgene, Manuela Preda worked at Kendle GmbH. She started as a Safety Specialist (I, II, Senior) from 2004 to 2010, spanning a total of 6 years. In 2010, she was promoted to Drug Safety Manager, a role she held for 10 months. Her experience at Kendle helped build her foundational skills in drug safety and risk management.
Academic Background and Qualifications
Manuela Preda has a robust academic background in pharmaceutical sciences and biopharmacy. She earned her Doctorate in Pharmaceutical Sciences from Université Joseph Fourier (Grenoble I). In addition, she holds a degree in Pharmacy and a Doctorate in Biopharmacy and Pharmakokinetic from the University of Medicine and Pharmacy Cluj Napoca, Romania. Her strong academic credentials have provided a solid foundation for her extensive career in the pharmaceutical industry.
Experience in Academia
Manuela Preda spent 11 years as an Assistant Professor at the University of Medicine and Pharmacy Cluj Napoca. Her role in academia from 1991 to 2002 involved teaching and contributing to the development of future pharmacists. This experience solidified her expertise in the pharmaceutical field and enriched her understanding of drug safety and medical information.