Zoe Radojicic

Clinical Research Coordinator @Memorial Sloan Kettering Cancer Center

Multiple Myeloma Service • Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information and present this information at regular research staff meetings. • Ensure strict compliance with IRB protocols and FDA regulations, maintaining meticulous records and facilitating audit-ready documentation. • Collaborate seamlessly with healthcare professionals, fostering effective communication and a harmonious working environment. • Thoroughly update changes in patient condition, adverse events, concomitant medication use, protocol compliance, and response to study drug.