Kristin Miller

Regulatory Affairs Coordinator @ Velocity Clinical Research

About Kristin Miller

Kristin Miller is a Regulatory Affairs Coordinator with extensive experience in clinical research and quality control. She has worked at Velocity Clinical Research, Inc. since 2021 and previously held various roles at Vitalink Research and Lexington Medical Center.

Current Role at Velocity Clinical Research

Kristin Miller serves as a Regulatory Affairs Coordinator at Velocity Clinical Research, Inc. since 2021. In this role, she is responsible for ensuring compliance with regulatory requirements and supporting the development of clinical research projects. Additionally, she holds the position of Quality Control Specialist at the same organization, where she focuses on maintaining quality standards in clinical trials.

Previous Experience at Vitalink Research

Kristin Miller has a history of working at Vitalink Research in various capacities. She began as a Clinical Research Assistant from 2017 to 2018 for nine months, followed by a role as Clinical Research Coordinator in 2018 for ten months. In 2021, she briefly served as a Regulatory Affairs Coordinator for three months and worked as a Quality Control Specialist from 2018 to 2021 for three years.

Experience at Lexington Medical Center

Prior to her roles in clinical research, Kristin Miller worked at Lexington Medical Center as a Pathology Support Tech II from 2014 to 2017 for three years. This position involved supporting pathology operations and contributing to the efficiency of laboratory processes in West Columbia, South Carolina.

Educational Background

Kristin Miller studied at Tri-County Technical College, where she earned an Associate of Science degree from 2008 to 2010. She then attended Clemson University, achieving a Bachelor of Arts in Biological Sciences from 2010 to 2013. Earlier, she completed her high school education at Gilbert High School from 2004 to 2008.

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