Brittany Mercante

Background

About Brittany Mercante

Clinical research professional with 10+ years of experience working in clinical research & the health care industry. I am well versed in Leadership and Management, Project Management, Clinical Research Operations, Institutional Review Board (IRB) requirements, Clinical Trial Management, CTMS, EDC, and Microsoft Office Suite. I have also worked extensively with CROs, pharmaceutical sponsors, external vendors, Principal Investigators, and clinical teams in various medical specialties. I currently have 8 years of experience in oncology research and am passionate about making a positive impact on the patients enrolled in clinical trials. I have extensive experience assisting the start-up of clinical trials and overseeing the day to day operations. I also have experience managing regulatory and compliance, adhering to federal and institutional guidelines, and leading a team of successful data coordinators. I previously worked as a clinical research coordinator and am experienced in extracting data from Electronic Health Records (EHR) and entering data, quality assurance and regulatory requirements governing human subjects research.