I most enjoy working with multidisciplinary teams to design projects, navigate the complex regulatory and administrative landscape governing medical research, and build the systems necessary to support the endeavor. In my work as an independent research consultant, I help startup companies ensure compliance with FDA mHealth, marketing and social media requirements for health products. I also work with researchers to take studies involving human subjects from conception to IRB approval, provide audit support, and develop SOPs to maintain research in compliance with the Common Rule, HIPPA, Medicare National Coverage Determination, GCP Guidelines, and other governing regulations.