Dainelle Clark has experience in quality, compliance, and regulatory affairs in both private and government sectors. In 2018, she joined the Food and Drug Administration (FDA) as a biologist, where she conducted compliance and quality assessments and surveillance for medical devices. Currently, Dainelle serves as a lead project manager in the Office of Policy for regulated drugs. She collaborates closely with project management and multi-disciplinary teams to develop policies and standards. Additionally, she is a member of the leadership team and contributes to the development and implementation of office policies and procedures, process improvements, and strategic planning initiatives. Dainelle holds a Doctor of Public Health, a Master of Science in biomedical science and regulatory compliance, and a Bachelor of Arts in biology with a minor in chemistry. She is certified as a Project Management Professional (PMP) and earned a Regulatory Affairs Certification (RAC) and Certified Associate in Health Information and Management Systems (CAHIMS).