Passionate and detail-oriented Clinical Research Professional with 15 month of experience in managing and coordinating clinical trail in centralized clinical research site. Skilled in patient recruitment,data management,and maintaining strong sponsor relationship. and ensuring compliance with all regulatory requirements.I am well-versed in ICH-GCP(R2) guidelines, NDCT 2019 guidelines and IRB protocol.Worked in centralized clinical research facility and had conduct phase 3 sponsor trial at site independently along with investigator initiated study