Madie Segna

Madie Segna brings a strong background in clinical operations and project management. She coordinates program management initiatives, providing support through various stages of development including clinical operations, clinical pharmacology, nonclinical studies, and business development.

Madie interacts with both internal and external stakeholders involved in clinical trials and nonclinical studies, overseeing the activities of vendors, CROs, and site personnel. Her ability to drive timelines and budgets for key functional deliverables is highly valued, and she collaborates closely with the Chief Medical Officer and Clinical Leadership Team to manage the Scientific Advisory Board and multiple Key Opinion Leaders. Madie also plays a key role in business development and due diligence activities, directly supporting the CEO and CBO by coordinating strategic meetings, managing data rooms and facilitating asset evaluation.

Prior to her current role, Madie worked at Medpace in Cincinnati, OH, where she held several positions, including Lead Clinical Research Project Coordinator. She specialized in cardiovascular, renal, metabolic, and medical device studies.

Madie holds a B.S in Biology from Xavier University. In her spare time, Madie enjoys traveling, watching reality tv, and playing golf.