Position Summary This position is responsible for directing the operational and strategic activities of the Global Regulatory Affairs organization for Palisade Bio. The incumbent will be responsible for ensuring that Palisade Bio’s Regulatory Affairs Function is robust, integrated to the company’s businesses, focused on enabling new product introductions, and will support the governance processes for regulatory affairs in alignment with regulatory requirements. The incumbent must have a comprehensive understanding of FDA/EU/ICH requirements, principles, concepts, industry practices, and standards.  In this hands-on role, s/he manages, reviews and edits the preparation of regulatory documents.  Duties include preparing, reviewing, and editing of clinical trial appl