Katherine Kim, Pharm.D.
About Katherine Kim, Pharm.D.
Katherine Kim, Pharm.D., is the Associate Director of Commercial Regulatory Affairs at Bristol Myers Squibb, with over 10 years of experience in the pharmaceutical industry.
Company
Katherine Kim, Pharm.D., currently holds the position of Associate Director, Commercial Regulatory Affairs at Bristol Myers Squibb. She joined the company in Summit, NJ, and has served in various capacities, displaying her extensive expertise in the pharmaceutical sector.
Title
As Associate Director, Commercial Regulatory Affairs at Bristol Myers Squibb, Katherine Kim is responsible for overseeing regulatory advertising and promotional activities, ensuring that all materials comply with FDA and other industry regulations.
Education and Expertise
Katherine Kim earned her Doctor of Pharmacy degree from the University of the Sciences in Philadelphia. With over 10 years of experience in Medical Communications/Medical Affairs and Ad Promo Medical Review, she possesses profound expertise in multiple therapeutic areas such as meningococcal disease & vaccines, prostate cancer, urology, overactive bladder, nephrology, hormone replacement, reproductive health, women’s health, GI, and OTC products.
Background
Katherine Kim has a robust background in the pharmaceutical industry. She worked at Alexion Pharmaceuticals, Inc. as Associate Director, Global Medical and Clinical Review from 2015 to 2018 in New Haven, CT. Prior to that, she served as Senior Manager, Medical Communications at Novartis Vaccines from 2014 to 2015 in East Hanover, NJ. Early in her career, she was Manager, Medical Communications at Actavis for six years. Her career showcases her extensive knowledge and skills in medical communications and regulatory affairs.
Achievements
Katherine Kim has consistently demonstrated expertise in handling unsolicited inquiries from healthcare professionals, and in the collection, analysis, and interpretation of clinical/scientific data. She has successfully managed external vendors and provided internal training to comply with company policies and standard operating procedures. Her experience working with cross-functional teams and her strong understanding of FDA industry regulations and pharmaceutical standards highlight her professional capabilities.