Matthew Palin
About Matthew Palin
Matthew Palin is a Principal Preclinical Research Associate at Boston Scientific with expertise in regulatory submissions, GLP, and preclinical device investigation.
Title and Current Position
Matthew Palin is currently serving as the Principal Preclinical Research Associate at Boston Scientific. He has been working in this role since 2012, bringing more than a decade of experience in preclinical research to the company. His work is primarily based in Minneapolis.
Professional Experience
Matthew Palin has extensive professional experience in the medical device industry. Prior to his current role at Boston Scientific, he worked at Surpass, Inc. as a Scientist/Study Director from 2011 to 2012. He also served as an Associate Research Scientist at Medtronic from 2003 to 2011. Throughout his career, Palin has focused on preclinical research, regulatory submissions, and managing studies and projects in the medical device sector.
Education and Credentials
Matthew Palin holds a Master's of Biotechnology from The Johns Hopkins University, achieved between 2013 and 2016. Additionally, he earned a Bachelor of Applied Science (B.A.Sc.) in Zoology/Animal Biology from the University of Wisconsin-Madison, where he studied from 1998 to 2002. His academic background has provided a solid foundation for his work in preclinical research and medical device development.
Expertise in Medical Device Industry
Matthew Palin possesses expertise in regulatory submissions and Good Laboratory Practice (GLP) within the medical device industry. His skills include interventional and surgical procedures, as well as imaging techniques. He has a strong background in anatomy and clinical development, which he utilizes in his role in preclinical research. His work often involves using animal models for preclinical device investigation.
Background in Preclinical Research
Matthew Palin has a demonstrated history of managing studies and projects in the medical device sector. His experience includes working with animal models, contributing to regulatory submissions, and adhering to Good Laboratory Practice (GLP) standards. His role often involves conducting interventional and surgical procedures, as well as employing various imaging techniques to advance preclinical device investigations.