Responsible for the smooth running of clinical trials in the division of Pediatric Infectious Disease.– Participant recruitment and screening– Data collection and maintaining details records of studies as per FDA guidelines– Adhering to research ethical and regulatory standards– Liaising with site monitors, sponsoring agencies, and laboratories to ensure compliance– Collaborating with PI and sponsoring agency to implement approved recommendations– Monitoring study participants to ensure adherence to study rules

I worked on the REGARDS C4R project that collected data regarding COVID-19 and it’s effects from over 6000 participants across the United States. I was responsible for importing the data into REDCap Data Management System.