Sally Duffy

Sally Duffy

Fellow, Safety Trial Manager @ Boston Scientific

About Sally Duffy

Sally Duffy is a Fellow and Safety Trial Manager at Boston Scientific Corporation with extensive experience in cardiac ablation studies and cardiac rhythm management devices.

Title and Current Role

Sally Duffy holds the title of Fellow, Safety Trial Manager at Boston Scientific Corporation. She has held this position since 2017. Her current role is home-based in the USA, focusing on ensuring the safety and efficacy of clinical trials within the company. Sally plays a crucial role in overseeing safety protocols and implementing regulatory requirements.

Professional Experience at Boston Scientific

Sally Duffy has a long-standing career at Boston Scientific Corporation, starting in 2004. Throughout her tenure, she has held multiple positions, including Principal Safety Trial Manager (2013-2017), Senior Lead CRA (2012-2013), Field Clinical Engineer (2008-2012), and Senior Clinical Research Associate (2004-2007). Her extensive experience within the company highlights her dedication and depth of knowledge in clinical trial management and safety oversight.

Previous Roles

Before her extensive career at Boston Scientific Corporation, Sally worked as a Clinical Research Associate at Guidant Corporation from 2003 to 2008. She also served as a Research Coordinator at Stern Cardiovascular Center from 1997 to 2003. Prior to transitioning into clinical research, Sally worked as an Emergency Room Nurse at Baptist Hospital, Memphis, Crittenden Hospital, AR, and various UK hospitals from 1990 to 1996.

Educational Background and Qualifications

Sally Duffy completed her studies at the University of Brighton, where she earned a Diploma in Registered Nursing from 1987 to 1990. Her robust educational background laid the foundation for her extensive career in clinical research and safety trial management.

Specialized Expertise and Focus Areas

Sally Duffy has a comprehensive understanding of Medical Device Coordination Group (MDCG) regulations, especially those implemented in May 2021. She is responsible for training team members on the rapidly changing EU regulatory reporting requirements. Additionally, she leads cross-divisional objectives and collaborates with various clinical functions to ensure consistent safety oversight. Currently, Sally focuses on cardiac ablation studies and has significant experience with cardiac rhythm management devices.

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