Drive the global regulatory strategy for pioneering CAR-T therapies, engaging with health authorities to ensure timely filings and approvals while addressing risks and fostering collaboration across teams to advance treatment access for patients.

Develop and execute innovative global regulatory strategies for CAR-T therapies, leading regulatory interactions, managing submissions, and ensuring compliance with health authorities to enhance patient access to transformative treatments.

Shape the future of cell therapy by providing essential CMC regulatory expertise across the product lifecycle, collaborating with multidisciplinary teams to drive submissions and maintaining compliance with regulatory standards.

Shape the future of clinical development by collaborating with cross-functional teams to design, monitor, and oversee innovative cell therapy trials while ensuring regulatory compliance and scientific rigor in a dynamic environment.

Accelerate progress at the forefront of clinical development, overseeing trials with a focus on regulatory compliance and scientific integrity. Collaborate cross-functionally to drive innovative cell therapies, ensuring patient safety and data accuracy.