Emily Scheese is a Clinical Research Associate (CRA) with experience in Phase I–III solid tumor oncology trials and neurology research. She previously served as an early phase clinical research coordinator specializing in early phase, solid tumor oncology. Her experience in both site and monitoring roles informs her approach to participant protection, protocol compliance, and site collaboration. In addition to her CRA responsibilities, Emily serves as a mentor to new CRAs and a data quality subject matter expert, helping colleagues strengthen data integrity and inspection readiness. She is passionate about improving patient safety through building strong site-sponsor relationships, process improvement, and practical education for clinical researchers. 

Arianna Carrizo-Korley, MHA, CCRP, is a regulatory leader with over six years of experience in clinical research, regulatory operations, and quality management. In addition to her master’s degree and certification of clinical research professional, Arianna is currently undergoing her doctoral studies in Healthcare Administration. Thus, she brings a unique combination of clinical research expertise, regulatory knowledge, and healthcare leadership to advancing compliant and efficient research operations. Arianna is experienced in leading regulatory teams, strengthening IRB and sponsor compliance, and developing standard operating procedures and training programs. Her efforts are also focused on conducting internal audits, supporting inspection readiness, and implementing process improvements aligned with FDA, NCI, sponsor, and institutional requirements. Known for a coaching-focused leadership style, Arianna is passionate about shaping research professionals, improving operational workflows, and building sustainable quality systems. Her approach emphasizes practical solutions, transparent communication, and scalable processes that promote both regulatory compliance and high-performing clinical research teams.

Jennifer Kinsey, CCRP, is an Oncology Clinical Operations Program Manager with five years of experience in oncology clinical research. Throughout her career, she has overseen the operational management of more than 150 Phase I-III clinical trials, supporting the successful execution of complex research studies. Jennifer earned her Bachelors in Exercise and Sport Science from the University of North Carolina at Chapel Hill and has been a Certified Clinical Research Professional for the past two and a half years. She is dedicated to advancing cancer research through high-quality clinical trial operations, regulatory compliance, and fostering a patient centered research environment