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Shannon Strom
Vice President and Head of Regulatory Affairs at Satsuma Pharmaceuticals, Inc.
Professional Background
Shannon Strom is a dedicated and accomplished leader in the field of drug development and regulatory affairs, renowned for her expertise and integrity in the industry. With a solid track record in formulating and executing global regulatory strategies, she possesses extensive experience in project management and clinical development, marking her as a highly respected figure in her field. Her career has been characterized by her strong ability to lead innovative teams and manage key responsibilities associated with global regulatory submissions and compliance.
As the Vice President and Head of Regulatory Affairs at Satsuma Pharmaceuticals, Inc., Shannon has played a pivotal role in shaping the company's regulatory strategy and ensuring the successful launch of new therapies. Her contributions extend beyond daily operations to include the development of comprehensive regulatory submissions, ensuring that new drug applications meet the stringent requirements set forth by health authorities worldwide.
Prior to her current role, Shannon served as the Senior Director of Global Regulatory Affairs at Roivant Sciences, where she was instrumental in navigating complex regulatory landscapes and implementing efficient strategies that aligned with the company's objectives. With her background as Senior Director and Director of Regulatory Affairs at Pearl Therapeutics, she has amassed a wealth of experience managing regulatory processes for various therapeutic areas.
Shannon’s professional journey began at Cato Research, where she honed her regulatory skills as an Associate Director of Regulatory Operations and a Senior Regulatory Scientist. Her involvement with Cato Research equipped her with a strong foundation in regulatory submissions, enhancing her analytical and strategic thinking abilities.
Education and Achievements
Shannon Strom's academic credentials are equally impressive. She earned her PhD in Pharmacology from the prestigious University of North Carolina at Chapel Hill, a program recognized for its robust research-oriented curriculum and training in pharmacological science. This advanced education laid the groundwork for her thorough understanding of drug action mechanisms and regulatory landscapes.
Furthermore, she completed her B.S. in Biology at Duke University, where she developed a passion for scientific inquiry and the complexities of biology, particularly in relation to drug development. This dual educational background has empowered Shannon to approach regulatory challenges from a scientific and strategic perspective, enabling her to implement effective solutions throughout her career.
Shannon’s specialties in global regulatory strategy, electronic regulatory submissions, and drug development are complemented by her strong project management skills, which make her a valuable asset in any organization.
Achievements
Throughout her outstanding career, Shannon Strom has garnered numerous achievements that showcase her expertise and commitment to advancing public health through effective drug regulation. Her successful leadership in securing global regulatory approvals has been vital in bringing innovative therapies to patients, thereby making a significant impact on healthcare.
Her innovative mindset has led to the successful implementation of efficient electronic regulatory submissions that streamline the approval process while ensuring compliance with regulatory guidelines. Shannon's adeptness at synthesizing regulatory requirements into actionable strategies has earned her a reputation as a go-to expert in regulatory affairs.
In addition to her professional roles, Shannon is committed to fostering the next generation of regulatory affairs professionals. She often engages in mentoring junior staff and contributing to educational initiatives within her industry, ensuring that her invaluable knowledge and experience are passed onto others.
With her extensive background in drug development and regulatory affairs, Shannon Strom continues to contribute significantly to the pharmaceutical industry, making her an influential figure in fostering successful drug development processes that benefit patients and healthcare providers alike.