Elena Alferova
Clinical Research Regulatory Coordinator II
UCSD Moores Cancer Center
I am a clinical research and regulatory professional with over 17 years of experience supporting oncology trials across academic, hospital-based, and industry settings. Currently, I work as a Research Regulatory Coordinator at UCSD Moores Cancer Center, where I manage regulatory submissions and ensure compliance for interventional oncology studies. Previously, I served as a Regulatory Manager at Novartis, where I was responsible for clinical trial regulatory strategy and submissions across multiple countries. I also held a regulatory role at Rady Childrens Hospital in San diego, supporting IRB and FDA interactions and helping implement institutional safeguards for patients protection. I hold a Master of Science in Drug Development and Product Management from UC San Diego and am a Certified Clinical Research Professional (CCRP) through SOCRA. My work focuses on aligning regulatory processes with ethical standards to support safe and effective clinical research.