Suzanne Courtney

Suzanne has been with Premier Research since 2005 and is currently an associate project director in the MedTech group. Prior to her current role, she has held positions of increasing scope and responsibility including Quality Assurance Auditor, Biometrics Associate, and escalating positions within Project Management, including a focus on management of medical device projects. Prior to joining Premier Research, Suzanne was an independent consultant providing various regulatory, clinical, and quality services to medical device manufacturers in the US and in Europe, including development of regulatory strategies, quality systems and procedures, and facility inspection preparation. She held the position of Director, Regulatory and Quality Affairs for EDAP Technomed, Inc. and Manager, Regulatory and Quality Affairs for Dornier Medical Systems (Dornier MedTech USA) writing regulatory submissions, overseeing international manufacturing as well as preparing for and hosting successful FDA inspections at both international facilities. Suzanne brings experience in endocrine/metabolic indications and specifically in diabetes, as well as experience in analgesia, cardiology, dermatology, genitourinary, infectious disease, oncology, orthopedics, pediatrics, pulmonology, psychiatry, general and cosmetic surgery, and additional experience in radiation therapy delivery systems.