Sally Linda
About Sally Linda
Sally Linda is a Senior Clinical Specialist at Boston Scientific with extensive experience in clinical research and regulatory affairs.
Professional Title
Sally Linda is currently a Senior Clinical Specialist at Boston Scientific. She started in this role in 2017, bringing significant experience in clinical research and regulatory affairs to the position in Marlborough, Massachusetts, United States.
Experience at Boston Scientific
Sally Linda has been a Senior Clinical Specialist at Boston Scientific since 2017. Her role involves significant responsibilities in clinical research, including the development and testing of Case Report Forms (CRFs) for various clinical trials. She collaborates closely with cross-functional groups such as Regulatory, Quality, Research and Development, and executive leadership to ensure comprehensive clinical trial management.
Previous Roles in Clinical Research
Before joining Boston Scientific, Sally Linda worked at Nuvectra from 2016 to 2017 as a Senior Clinical Affairs Specialist in Plano, Texas. She was a Clinical Research Associate II at St. Jude Medical from 2014 to 2016 in Minnesota, and a Clinical Research Associate in Neuromodulation at Medtronic in 2014 for 9 months. Additionally, she served as a Clinical Research Specialist at Apnex Medical, Inc. from 2011 to 2013.
Earlier Career in Chemistry and Clinical Trials
Sally Linda's career began in chemistry, working as an Intermediate Chemist at Pace Analytical from 1999 to 2001 in Minneapolis and as a Chemist I at IBP from 1996 to 1999 in Huntsville, Alabama. She transitioned into clinical research at DaVita as a Research Assistant from 2001 to 2002 in Denver, Colorado, and later, as a Clinical Trials Project Manager at Multidata from 2002 to 2004.
Educational Background
Sally Linda earned a Bachelors in Biology from the University of Northern Iowa, completing her degree from 1994 to 1999. Her education laid the foundation for her extensive career in clinical research, regulatory affairs, and chemistry.
Regulatory Expertise
Sally Linda has a strong background in working with EU Regulatory Bodies, particularly within the scope of MEDDEV guidelines. She has a comprehensive understanding of GCP/ICH/FDA regulations, which supports her role in ensuring compliance in clinical trials and regulatory submissions.