Nikki Cammarata has nearly a decade of experience in conducting early and late phase clinical trials. From her experience acting in traditional Clinical Operations roles, such as a Clinical Trial Manager, she transferred this skillset and knowledge to prioritize work on Clinical Quality projects. She has experience conducting audits, completing gap assessments, supporting regulatory authority inspections, and developing Standard Operating Procedures (SOPs). She also uses her project management skills to implement clinical systems (e.g., CTMS and eTMF). Nikki’s role at Halloran is to use her experience within Clinical Quality and Compliance to deliver accurate and efficient services to clients

Prior to joining Halloran, Nikki worked as a Site Management Associate (SMA) at ICON Clinical Research, a contract research organization. As a SMA, Nikki acted as an in-house clinical research associate supporting Principal Investigators across the country that were enrolling patients in multiple late-phase studies. In this role, Nikki was responsible for the accuracy of the information and data contained in the Electronic Data Capture (EDC) systems, Clinical Trial Management System (CTMS), and Interactive Response Technology (IRT) systems. Before ICON, Nikki worked as a Senior Research Coordinator at Ophthalmic Consultants of Boston, where she managed the execution of numerous early-phase studies.

Education:
Northeastern University, Bachelor of Science, Biology