Karen Salovich, Senior Director of Regulatory Operations. Karen has over 20 years of experience in Biopharmaceutical Regulatory Operations. She brings extensive experience in eCTD publishing and leading the Regulatory dossier preparation, publishing and submissions of multiple application types, including US INDs, BLAs and global MAAs. Karen has excelled in Regulatory Operations at a broad range of pharma and vaccine companies including Novavax, Arcellx, Human Genome Sciences, and Shire Pharmaceuticals. Prior to joining ILiAD, Karen was the Director of Regulatory operations at Vaxxinity, where she effectively managed the publishing of a Marketing Application to the MHRA and TGA simultaneously and managed the publishing of multiple INDs to the FDA to support all programs. Her experience also includes a consultant role at Parexel International where she was a Subject Matter Expert and Project Lead in the management, production and delivery of regulatory submissions for clients. Karen holds a Bachelor of Science degree from Radford University.