Jennifer Grohman
About Jennifer Grohman
Jennifer Grohman is the Associate Director, Labeling Lead, Labeling Strategy at Bristol-Myers Squibb and Associate Director Regulatory Affairs at Ferring Pharmaceuticals.
Current Positions at Bristol-Myers Squibb and Ferring Pharmaceuticals
Jennifer Grohman currently holds the position of Associate Director, Labeling Lead, Labeling Strategy at Bristol-Myers Squibb in Princeton, NJ. In this role, she co-leads the development and maintenance of the Company Core Data Sheet (CCDS), the US Package Insert (USPI), and the EU Summary of Product Characteristics (EU-SmPC). Simultaneously, she works as an Associate Director Regulatory Affairs at Ferring Pharmaceuticals in the Greater New York City Area, where she provides strategic and operational support to local markets in handling Health Authority (HA) labeling requests.
Past Roles in Regulatory Affairs and Labeling
Jennifer Grohman has extensive experience in regulatory affairs and labeling. She served five years as Associate Director, Labeling at Sandoz in East Hanover, NJ, and three years as Senior Manager, Labeling Global Regulatory Affairs at Bausch + Lomb in Madison, NJ. Prior to that, she held the position of Regulatory Affairs Labeling Manager at Bayer HealthCare Pharmaceuticals, Inc for three years. She began her career in regulatory affairs as a Regulatory Affairs Labeling Analyst at B. Braun Medical Inc and previously worked at Wyeth - Wyeth Consumer Healthcare.
Experience at Nabisco and Educational Background
Before transitioning into regulatory affairs, Jennifer Grohman worked as a Continuous Improvement Coordinator at Nabisco. Academically, she holds a Bachelor of Arts in English Writing and Literature from William Paterson University of New Jersey, having completed her studies from 1995 to 2000. She also attended the Chubb Institute of Technology, where she earned a diploma in Graphic Design and Development.
Labeling Strategy Expertise
In her role at Bristol-Myers Squibb, Jennifer Grohman is heavily involved in forming labeling strategies. She participates on global and regional regulatory and project development teams to identify, evaluate, and provide operational guidance on labeling issues. Her responsibilities include creating labeling strategies based on business objectives, data, and regulatory requirements. She coordinates the internal labeling approval process as per standard operating procedures and provides expertise on label content requirements, standards, and processes.
Leadership in Label Content Development
Jennifer Grohman has demonstrated leadership in labeling content development. She plans and moderates meetings to discuss and develop label content, including defining agendas and taking minutes. Her role encompasses substantial contributions to drafting and maintaining critical labeling documents such as the Company Core Data Sheet (CCDS), US Package Insert (USPI), and the EU Summary of Product Characteristics (EU-SmPC).