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Deborah (Deb) Morris is Senior Regulatory and Clinical Affairs Advisor at Cue Health, a health technology company whose mission is to enable personalized, proactive, and informed healthcare that empowers people to live their healthiest lives.

Deb provides leadership and direction for regulatory and clinical affairs at the company. She develops regulatory strategies, manages regulatory submissions, leads interactions with regulators, and directs and manages the clinical team in the design and execution of compliant, on-budget, and timely clinical studies.

Deb has over 40 years of experience in executive management and her expertise includes clinical and regulatory strategies for in-vitro diagnostics, clinical operations, protocol development, clinical trial management, data analysis, and the U.S. and international regulatory submissions. Prior to Cue, she served as Senior Director, Clinical for Myraqa, a wholly-owned subsidiary of Illumina Inc.; Director, Regulatory Affairs Strategic Initiatives at GE Healthcare; and Senior Director, Clinical and Regulatory Affairs at Focus Diagnostics. Deb began her career at Ischemia Technologies and served in various clinical and regulatory affairs roles at Siemens Healthcare.

Deb earned Master of Science degrees in biostatistics from New York Medical College and computer science from New York University. She also holds a Bachelor of Arts degree in biology from the State University of New York at Albany.