Yasuoka Yuka
About Yasuoka Yuka
Yasuoka Yuka is a Senior Manager at Bristol-Myers Squibb, specializing in Product Assurance and Pharmacovigilance in Japan, with over 15 years of experience in the pharmaceutical industry.
Current Position at Bristol-Myers Squibb
Yasuoka Yuka currently serves as the Senior Manager at Bristol-Myers Squibb in the Pharmaceutical Officer Office, Product Assurance and Pharmacovigilance, Japan. In this role, she is responsible for overseeing product assurance and ensuring pharmacovigilance compliance within the Japanese market. Her extensive background in safety management and clinical medicine supports her contributions to the company's ongoing efforts in maintaining high standards of drug safety.
Previous Roles at Bristol-Myers Squibb
Yuka's career at Bristol-Myers Squibb spans over a decade and includes multiple senior management positions. These roles include Senior Manager of Immuno-Oncology Safety Management Office in Product Assurance (2016-2017), Senior Manager of Safety Strategy in Medical and Pharmacovigilance R&D, Japan (2012-2016), and Senior Manager of RMP Design in Medical and Pharmacovigilance R&D, Japan (2011-2012). She also had a significant role in the Medical Information department focusing on Immunology from 2008 to 2011.
Experience at Kameda Medical Hospital
Before her extensive tenure at Bristol-Myers Squibb, Yuka worked at Kameda Medical Hospital. She served as a Clinical Pharmacist in 2007 for eight months and as a Pharmacy Resident from 2005 to 2007. This early clinical experience laid the groundwork for her deep expertise in pharmacovigilance and medical information management.
Educational Background
Yuka graduated from Kitasato University with a degree from the Department of Clinical Medicine, School of Pharmacy. This education provided her with a robust foundation in clinical medicine and pharmacy, essential for her subsequent roles in pharmacovigilance and product assurance in the pharmaceutical industry.
Expertise in Pharmacovigilance and Product Assurance
With over 15 years of experience in the pharmaceutical industry, particularly in pharmacovigilance and product assurance, Yuka has developed a deep understanding of drug safety and risk management. Her work has consistently focused on safety strategy, Risk Management Plan (RMP) design, and ensuring compliance with pharmacovigilance regulations. Her career reflects a transition from hands-on clinical roles to strategic management positions, demonstrating her expertise and adaptability in the field.