Morgan K. Foret

Background

About Morgan K. Foret

Passionate and dedicated industry professional with expertise in regulatory submissions, neuroscience, and preclinical (GLP) toxicology and safety pharmacology study management, specializing in central nervous system gene therapies. Able to adapt quickly to different environments and thrives on new challenges. Self-motivated, capable of working independently or collaboratively towards meeting tight deadlines for client CTA, IND/equivalent applications. Extensive interpersonal and communication skills built through regulatory authority-facing project management, client-facing project management and through authoring IND non-clinical sections, study protocols/amendments, SOPs, non-clinical reports, and research results (manuscripts, reviews, abstracts, grant applications, posters and oral presentations). Overall, guided by a solution-oriented approach and eager to contribute to bettering the lives of patients.