Tajneen Natasha
About Tajneen Natasha
Tajneen Natasha is the Director, Business Operations Lead, Medical Capabilities at Bristol-Myers Squibb, with over 15 years of experience in R&D operations within the pharmaceutical and consulting industries.
Title and Current Role
Tajneen Natasha holds the title of Director, Business Operations Lead, Medical Capabilities at Bristol-Myers Squibb. Based in Princeton Pike, NJ, she oversees business operations related to medical capabilities. Her role involves strategic planning and optimization of R&D operations, ensuring effective collaboration across various departments.
Previous Experience at PwC
From 2014 to 2017, Tajneen Natasha served as Manager, Health Industries Advisory within the Pharmaceuticals & Life Sciences R&D Advisory Services at PwC in the Greater New York City Area. In this role, she leveraged her expertise to guide clients in the pharmaceutical sector, focusing on the design and implementation of R&D operating models and business processes.
Experience at Merck & Co. Inc.
Tajneen Natasha worked at Merck & Co. Inc. in various capacities. Between 2012 and 2013, she was a Finance Specialist – Grant Processor on a special assignment and a Project Manager in Global Regulatory Operations in Rahway, NJ. Previously, she served as Associate Research Scientist from 2007 to 2012 and as Research Biologist from 2005 to 2007 in Rahway, NJ and West Point, PA, respectively.
Educational Background
Tajneen Natasha earned an M.B.A. in Finance and Pharmaceutical Management from Rutgers, The State University of New Jersey-Newark, where she studied from 2010 to 2014. Prior to this, she obtained a degree in Biomedical Engineering from Rutgers, The State University of New Jersey-New Brunswick, completing her studies from 1999 to 2003.
Expertise in R&D Operations
With over 15 years of experience in end-to-end R&D operations, Tajneen Natasha has demonstrated expertise in strategic planning, optimization of R&D processes, and design of technology solutions. Her experience spans Clinical Research & Development, Medical Affairs, Regulatory Affairs, and Quality Assurance & Compliance. She is skilled at driving cross-functional initiatives and managing change for technical and process improvements.