Kelley C. Boyer, MS

Area of Expertise:

Kelley Boyer, MS

Kelley leads SciLucent’s regulatory operations practice where she provides regulatory guidance with a specific focus on regulatory submissions and assuring the completeness and quality of submissions from the operations perspective. She is responsible for all aspects of filing of high-quality submissions to FDA in both paper and electronic formats. She oversees the electronic submission of regulatory documents through FDA’s electronic gateway. Kelley is current pursuing a Ph.D. in Science and Technology Studies from Virginia Polytechnic and State University. She has an M.S. in Science and Technology Studies from Virginia Polytechnic and State and an M.S. in Technical and Scientific Communication from James Madison University. She has a B.S. in Biology with a minor in English from the University of Richmond.