Mamta Shetty

Mamta Shetty has extensive experience in clinical research and trial management, holding various leadership roles focused on Trial Master File and regulatory submissions. At ICON plc, responsibilities included overseeing the accuracy and quality of the Trial Master File across clinical trials. Previous positions spanned KEM Hospital as a Study Coordinator, where key responsibilities encompassed completing study documentation and ensuring participant welfare, and PPD, where tasks included conducting feasibility studies and managing regulatory document submissions. Additionally, Mamta held roles at Pharm-Olam, LLC, serving as a Senior Trial Master File Lead, contributing to the efficient management of clinical trial logistics and compliance. Throughout the career, a focus on collaboration with diverse stakeholders and adherence to regulatory standards has been central.