Maria Rhoades
About Maria Rhoades
Maria Rhoades is a Clinical Project Manager with extensive experience in clinical research and project management. She has worked for AtriCure, Inc. since 2014 and has held various roles in notable companies such as Interlace Medical, KV Pharmaceutical, and Hologic.
Work at AtriCure
Maria Rhoades has been employed at AtriCure, Inc. as a Clinical Project Manager since 2014. In this role, she oversees clinical projects, ensuring they are executed efficiently and meet regulatory standards. Her tenure at AtriCure spans 10 years, during which she has contributed to the development and management of clinical trials aimed at improving patient outcomes in cardiac care.
Previous Experience at Interlace Medical
Before joining AtriCure, Maria Rhoades worked at Interlace Medical. She initially served as a Project Manager from 2009 to 2010, where she was responsible for coordinating project activities. Subsequently, she returned to Interlace Medical as a Senior Clinical Research Associate Project Manager from 2009 to 2011, managing clinical research initiatives and ensuring compliance with industry standards.
Experience at KV Pharmaceutical
Maria Rhoades worked at KV Pharmaceutical as a Clinical Research Associate III from 2007 to 2009. In this position, she was involved in monitoring clinical trials and ensuring adherence to regulatory requirements. Her experience at KV Pharmaceutical equipped her with the skills necessary for managing complex clinical research projects.
Role at Hologic
At Hologic, Maria Rhoades served as a Senior Clinical Research Associate from 2009 to 2014. During her five years at Hologic, she played a key role in conducting clinical trials, focusing on the development of medical devices and diagnostics. Her work involved collaborating with various stakeholders to ensure the successful execution of clinical studies.
Education and Expertise
While specific details about Maria Rhoades' educational background are not provided, her extensive experience in clinical project management and research indicates a strong foundation in clinical practices and regulatory compliance. Her roles across various organizations highlight her expertise in managing clinical trials and her ability to navigate complex project requirements.