Carie Masoner

Carie Masoner brings over 25 years of experience in the pharmaceutical, biotech, and Clinical Research Organization industries. She coordinates program management initiatives, providing support through various stages of development including clinical operations and regulatory affairs. Prior to joining JucaBio, Carie held positions of increasing leadership and responsibility, including Head of Global Regulatory and Scientific Affairs at CTI Clinical Trials & Consulting, Head of Regulatory and Medical Writing at Firma Clinical Research, Associate Director of Regulatory Affairs at Xanodyne Pharmaceuticals, Senior Clinical Trial Manager of Product Development at Xanodyne Pharmaceuticals, and Clinical Trial Manager and Lead CRA at Medpace.

Throughout her career, she has managed multiple global clinical programs, led the development and maintenance of Investigational New Drug (IND) dossiers, and successfully contributed to and submitted over 12 successful NDAs and BLAs. She has experience across therapeutic areas including metabolic diseases, pulmonary, infectious disease, oncology, transplant, pain, and rare diseases. The combination of her experience in Clinical Operations and Regulatory Affairs has provided her with a deep understanding of the complexity and needs in drug development, allowing her to excel at developing teams and operationalizing programs.

Carie holds a B.S. in Human and Consumer Science from Ohio University. In her personal life, Carie enjoys traveling, reading, playing games of skill and spending time with her family.