Lee Quist is a Clinical Development professional at Moderna, specializing in infectious disease vaccines with extensive experience leading global submissions, including IND, CTA, BLA, and MAA. They have effectively managed complex projects and cross-functional teams to drive regulatory approvals, particularly focusing on Phase 3 pivotal efficacy trials. Lee's background includes roles such as Regulatory Writer and Medical Writer, and they have contributed to medical communications and project coordination across various organizations. With a Master of Business Administration and a strong foundation in biology, Lee combines expertise in regulatory compliance and innovative technologies to advance therapeutic solutions in the life sciences sector.
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