Lise Alessio
About Lise Alessio
Lise Alessio is the Associate Director of Global Regulatory Sciences, Oncology at Bristol Myers Squibb in Neuchâtel, Suisse, with extensive experience in regulatory affairs across various pharmaceutical companies.
Company
Lise Alessio currently holds the position of Associate Director, Global Regulatory Sciences, Oncology at Bristol Myers Squibb in Neuchâtel, Suisse. Bristol Myers Squibb is a prominent global biopharmaceutical company committed to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. Her role emphasizes regulatory sciences within oncology, indicating a focus on the development and approval processes of oncology treatments.
Title
Lise Alessio is the Associate Director, Global Regulatory Sciences, Oncology at Bristol Myers Squibb. She consistently engages with global regulatory strategies and policies, ensuring that oncology assets meet rigorous regulatory standards. Her role involves coordinating with various stakeholders to navigate the complex regulatory environments worldwide, thus facilitating the availability of oncology treatments.
Education and Expertise
Lise Alessio completed her education at Paris-Sud University (Paris XI) where she earned a Master's degree in International Drug Development and Registration in 2014. She also obtained a Doctor of Pharmacy (PharmD) from Aix-Marseille University in 2014. Her educational background in pharmacy and international drug development has provided her with substantial knowledge and skills in regulatory sciences, essential for her current and previous roles in the pharmaceutical industry.
Career Background
Lise Alessio's career spans notable positions at various pharmaceutical companies. At Bristol Myers Squibb, she served in multiple roles including Senior Manager and Associate Director, covering global regulatory strategies and policies from 2021 to 2023. Prior to this, she worked at Celgene as a Senior Manager handling EU Regulatory Affairs - I&I. Her tenure at Allergan included managerial roles in regulatory affairs for various therapeutic areas. She started her career with student placements at ANSM and Bayer HealthCare, alongside internships at several hospitals and Sanofi.
Professional Experience
Throughout her professional journey, Lise Alessio has held several key roles at leading pharmaceutical firms. She headed regulatory affairs initiatives as a Senior Manager at Celgene and as an Associate Director at Bristol Myers Squibb, managing global regulatory compliance and strategies. Her earlier roles at Allergan involved regulatory affairs in gastrointestinal and clinical trials. Lise's extensive regulatory experience is rooted in her education and numerous internships, which provided practical insights into the pharmaceutical industry.