Cecilia Deterville
About Cecilia Deterville
Cecilia Deterville is a Senior Clinical Research Coordinator at NYU Langone Health, specializing in Phase 2 and Phase 3 clinical trials for liver and kidney diseases. She has extensive experience in clinical research coordination and health promotion, with a background in developing SOPs, preparing IRB submissions, and managing clinical trial budgets.
Current Role at NYU Langone Health
Cecilia Deterville holds the position of Senior Clinical Research Coordinator at NYU Langone Health, specifically at the Transplant Institute. She has been in this role since 2016. Her responsibilities include overseeing Phase 2 and Phase 3 clinical trials related to liver and kidney diseases such as hepatitis C (HCV), hepatocellular carcinoma (HCC), and antibody-mediated rejection (AMR). Deterville is tasked with managing day-to-day activities of clinical trials and supervising research staff.
Previous Experience at NYU Langone Health
Prior to her current role, Cecilia Deterville worked as a Clinical Research Coordinator at NYU Langone Health from 2012 to 2016 in the Greater New York City Area. During this period, she gained substantial experience in conducting clinical research, which laid the foundation for her subsequent promotion to Senior Clinical Research Coordinator.
Educational Background
Cecilia Deterville earned her Master of Science degree in Exercise & Health Studies: Health Promotion from Miami University, where she studied from 2010 to 2012. She also holds a Bachelor of Science degree in Health Science: Health Promotion from Ithaca College, completed in 2010. Her academic background provided a strong foundation in health promotion and research methodologies.
Clinical Trials Management and SOP Development
In her role at the Transplant Institute of NYU Langone Health, Cecilia Deterville is responsible for developing Standard Operating Procedures (SOPs) to ensure precise execution of research tasks. Additionally, she prepares Institutional Review Board (IRB) submissions, creates clinical trial budgets, and conducts Prospective Reimbursement Analysis. This comprehensive involvement in clinical trials underscores her expertise in both the organizational and financial aspects of clinical research.
Responsibility for Educational In-Services
Cecilia Deterville provides educational in-services to staff throughout the enrollment period of clinical trials. This involves training and guiding staff on the protocols and processes required for effective trial management, thereby ensuring adherence to regulatory and procedural standards. Her role in education underscores her commitment to maintaining high standards in clinical research practices.