Diane I.

Vice President, Regulatory Affairs

Professional Overview
Diane I. is an accomplished regulatory affairs executive with over 25 years of experience in the biotechnology and pharmaceutical industries. As the Vice President of Regulatory Affairs at Neumora Therapeutics, she leverages her deep expertise in navigating complex regulatory landscapes to drive the successful development and approval of innovative therapies.

Experience Summary

Current Role
As the Vice President of Regulatory Affairs at Neumora Therapeutics, Diane is responsible for leading the company's regulatory strategy and ensuring compliance with global regulatory requirements. She oversees the preparation and submission of regulatory applications, liaises with key regulatory authorities, and manages a team of regulatory affairs professionals to optimize the company's regulatory activities.

Career Progression
Prior to joining Neumora Therapeutics, Diane held senior regulatory affairs roles at several prominent biotechnology companies, including Tranquis Therapeutics, Jasper Therapeutics, Vir Biotechnology, and Dermira. In these positions, she demonstrated her ability to successfully guide drug candidates through the regulatory approval process, contributing to the successful launch of multiple therapeutic products.

Diane's career trajectory has been marked by progressive leadership responsibilities and a proven track record of driving regulatory excellence. Her industry contributions have been recognized through her involvement in various regulatory affairs professional organizations, where she has shared her expertise and best practices with her peers.

Academic Background
Diane holds a Bachelor of Science degree in Biological Sciences from the University of California, Davis, and a Master of Science degree in Regulatory Affairs from the University of Southern California.

Areas of Expertise

• Regulatory strategy development and execution

• Global regulatory submissions and approvals

• Navigating complex regulatory landscapes

• Stakeholder management and cross-functional collaboration

• Team leadership and talent development

• Regulatory compliance and risk mitigation

Professional Impact
Throughout her career, Diane has played a pivotal role in the successful regulatory approval of numerous innovative therapies, contributing to improved patient outcomes and advancing the field of biotechnology. Her deep understanding of regulatory requirements, combined with her strategic leadership and collaborative approach, have earned her a reputation as a highly respected and influential regulatory affairs expert.

Conclusion
With her exceptional regulatory expertise, proven track record of success, and unwavering commitment to driving innovation, Diane is poised to continue making a significant impact in the biotechnology industry. As the Vice President of Regulatory Affairs at Neumora Therapeutics, she is well-positioned to guide the company's regulatory efforts, contributing to the development and commercialization of groundbreaking therapies that address unmet medical needs.