Director, Regulatory Operations
Rebecca has over 15 years of experience in clinical research, focused within Clinical Research Organizations across multiple indications and phases. Originally entering the industry supporting regulatory affairs submissions, Rebecca quickly moved into Clinical Operations as a clinical research assistant, a CRA, and a Clinical Trial Manager. Identifying a passion for supporting and developing employees, Rebecca moved to line management roles with a focus on site start-up, project administration and eTMF, most recently leading a global team of managers, specialists, and associates at a mid-sized CRO. Rebecca has experience completing, overseeing, and continually improving upon site start-up and eTMF processes, has a secure understanding of regulation and industry standards, and works collaboratively across functions and with clients. Rebecca is dedicated to quality and efficiency, and strives to ensure that we consistently deliver superior, on-time support and materials for our clients.