Kathy Belfiore
About Kathy Belfiore
Kathy Belfiore serves as a Patient Liaison at Atlantic Health System, where she utilizes her strong communication skills to enhance patient satisfaction. With over 15 years of experience in quality control and medical writing, she has a background in both pharmaceutical research and customer service.
Work at Atlantic Health System
Kathy Belfiore has been serving as a Patient Liaison at Atlantic Health System since 2015. In this role, she focuses on identifying and communicating patient satisfaction improvement opportunities to management at Overlook Medical Center in Summit, NJ. Her responsibilities include assisting in the updating of administrative materials and resources to enhance patient information and comfort. Kathy's extensive experience in quality control and patient communication contributes to her effectiveness in this position.
Previous Experience in Pharmaceutical and Retail Sectors
Before her current role, Kathy worked at Schering-Plough Research Institute as a QC Specialist and Medical Writer from 2007 to 2010. She gained valuable experience in quality control consulting and medical writing during this time. Following that, she served as an Assistant Manager at Williams-Sonoma, Inc. from 2011 to 2015. These positions provided her with a diverse skill set applicable to her current role in patient liaison.
Education and Expertise
Kathy Belfiore studied at Katharine Gibbs School, where she achieved Certified with Honors in Secretarial/Business from 1976 to 1977. She also attended Fairleigh Dickinson University, focusing on Business/Science from 1979 to 1980. Her educational background supports her expertise in communication, quality control, and medical writing, which are essential in her role as a Patient Liaison.
Skills in Communication and Quality Control
Kathy possesses outstanding verbal and written communication skills, which are crucial for her role as a Patient Liaison. She has over 15 years of experience in quality control consulting, editing, and auditing clinical trials data and submission documents within the pharmaceutical and Contract Research Organization (CRO) environments. Her skills include editing and medical writing, supporting protocol design, and preparing regulatory documentation for NDA/IND submissions.