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Elaine Clark is an accomplished development professional with over 20 years of industry experience in a broad range of responsibilities within start-up biotech, CRO and global commercial organizations. She has extensive experience in interactions with global health authorities and supporting strategic planning and positioning of development stage assets, including recent experience with the dermatology division of the FDA. Prior to joining Dermavant, Ms. Clark was VP of Global Regulatory Affairs at PRA Health where she was responsible for regulatory CMC, labeling and emerging marketing activities for a portfolio of Takeda marketed products. Previously, she was Head of Global Regulatory Affairs at Galderma where she oversaw all regulatory activities within the prescription business unit. She directed successful global marketing applications for Mirvaso®, Soolantra®, and Epiduo® Forte. Ms. Clark was also Head of Regulatory Affairs for Lexicon Pharmaceuticals where she oversaw successful IND/CTA filings for seven first-in-class new molecular entities to enable first-in-human trials.