Vivian Lua, Pharm D
About Vivian Lua, Pharm D
Vivian Lua, PharmD, is a Global Feasibility Manager at Bristol Myers Squibb with a diverse background in pharmacy practice and pharmaceutical industry roles.
Current Role at Bristol Myers Squibb
Vivian Lua currently serves as the Global Feasibility Manager at Bristol Myers Squibb in New Jersey, United States. She joined the company in May 2020. In this role, she is responsible for overseeing the global feasibility of clinical trials, ensuring that trials meet regulatory requirements and operational timelines. Her position involves collaborating with various stakeholders to optimize study designs and execution plans.
Previous Experience at Covance
Vivian Lua worked as a Global Study Manager at Covance from 2018 to 2019 in the Geneva Area, Switzerland. During her tenure, she managed multiple global clinical studies, coordinating efforts across different regions to ensure the smooth execution of trials. Her responsibilities included overseeing study timelines, monitoring compliance with regulatory standards, and liaising with external partners.
Role at Boehringer Ingelheim
From 2016 to 2017, Vivian Lua held the position of Medical Affairs Associate at Boehringer Ingelheim in Dubai, UAE. In this role, she was involved in medical affairs activities, including the support of clinical development programs and the dissemination of medical information. She ensured alignment with regulatory frameworks and facilitated communication between medical teams and external stakeholders.
Educational Background
Vivian Lua obtained her Doctor of Pharmacy (PharmD) degree from the University of Connecticut from 2011 to 2013 after previously earning a Bachelor of Pharmacy from the same institution from 2007 to 2011. Her education provided her a comprehensive foundation in pharmacy practice and pharmaceutical sciences, equipping her with the knowledge and skills necessary for her diverse career in the pharmaceutical industry.
Early Career and Internships
Vivian Lua's early career involved roles such as Lab Assistant and Regulatory Affairs Intern at Huahai US, Inc., where she worked from 2009 to 2011 and for 3 months in 2010 in Cranbury, NJ. She also gained valuable experience as a Clinical Pharmacy Research Services Intern at Genzyme for 3 months in 2008 in Framingham, MA. These roles helped her build a strong foundation in regulatory affairs and clinical research before transitioning to more advanced positions in the pharmaceutical industry.