Wherever you are in your product development lifecycle,
Sterling can help.
Human Factors and Clinical Manager
Resource Manager Tara Miller has over 18 years of experience in the clinical research and medical device industries. Ms. Miller provides her expertise to clients to support their human factors evaluations throughout the medical device development process and post commercialization, regulatory submissions for market approval to governing bodies throughout the world, and regulatory compliance in the conduct of clinical studies. Ms. Miller has been an adjunct professor at Drexel University College of Medicine, Graduate School of Biomedical Sciences and Professional Studies since 2013, where she developed the curriculum for and teaches on clinical project management. She earned her Master of Science in Clinical Research Organization and Management from Drexel University College of Medicine and her Bachelor of Science in Business Management from the University of Phoenix. Ms. Miller finds reward in utilizing her experience and collaborating with design teams to optimize the user experience and develop products that are safe and effective.
July 29, 2022
February 18, 2021
September 8, 2020