At Parexel International, I facilitated site access to study systems, addressed site issues, and supported compliance with study training requirements. I also performed qualification and initiation visits and evaluated recruitment plans with site staff.
At Pharm-Olam, LLC, I performed site evaluation, initiation, interim monitoring, and close-out visits across clinical study phases. I also participated in study start-up by reviewing protocols, CRFs, and informed consent forms.
As a Business Solutions Consultant for Various Employers, I directed and maintained a targeted team supporting logistics coordination, documentation management, compliance, and quality assurance for private sponsors and contractors throughout the clinical trial life cycle.
My clinical trial experience spans areas including dermatology, digestive disease, diabetes, infectious disease, neurology, oncology, and ophthalmology. I hold a B.S. in Biology and an M.S. in Information Design and Strategy, with a Data Communication Specialization.
