Post-doctoral Research Fellow, CIDR (AUBMC) — surveillance data and study operations
During post-doctoral research at CIDR, contributed to multiple surveillance programs and studies requiring systematic handling of clinical/epidemiological data. Performed and supported data collection/entry and analysis using SPSS/Excel, enabling interpretation and downstream reporting. Assisted with regulatory and study materials preparation such as consent forms, case report forms, and accountability logs. • Supported primary immunodeficiency program development and screening-related data workflows. • Contributed to genetic and functional study datasets for primary immunodeficiency disorders. • Helped support severe acute respiratory infection and influenza hospital surveillance data handling. • Prepared study documentation including informed consent, CRFs, and enrolment/drug accountability logs.