Laura Kelly
About Laura Kelly
Laura Kelly is a Regulatory Affairs Specialist II at Boston Scientific with extensive experience in regulatory and clinical affairs.
Current Role at Boston Scientific
Laura Kelly has been working as a Regulatory Affairs Specialist II at Boston Scientific since 2015. In this role, she is involved in various regulatory processes, ensuring that products meet all necessary legal and regulatory requirements before they are distributed or sold. Her work involves close collaboration with product development teams to prepare and submit documentation required by regulatory bodies.
Previous Experience at Diagnostic Group LLC
Laura Kelly worked at Diagnostic Group LLC as a Regulatory Affairs Specialist from 2012 to 2015, totaling three years. During her tenure, she was responsible for preparing and managing regulatory submissions for new products and ensuring ongoing compliance with regulatory standards for existing products.
Role at Grason-Stadler
From 2011 to 2012, Laura Kelly served as a Documentation Coordinator at Grason-Stadler for one year. Her responsibilities included maintaining comprehensive documentation systems, ensuring the accuracy and completeness of regulatory documents, and supporting internal audits and regulatory inspections.
Position at Cardia Inc.
Laura Kelly was a Regulatory and Clinical Affairs Specialist at Cardia Inc. from 2006 to 2011, a period of five years. In this role, she was involved in both regulatory and clinical aspects, working on regulatory submissions and clinical trial documentation. Her work supported product approvals and clinical evaluations required for market access.
Educational Background
Laura Kelly completed her bachelor's degree at Hamline University, where she studied from 2001 to 2004. This education provided her with a foundation in regulatory affairs, preparing her for her subsequent roles in the medical device and healthcare sectors.