(Sr.) Clinical Research Associate

The position

The (Sr.) Clinical Research Associate (CRA) oversees site management for the selection, initiation, conduct, and closure of studies, ensuring compliance with local regulations, ICH-GCP, and Novo Nordisk procedures to maintain data quality and safety of study subjects. The (Sr.) CRA is in charge of the site-level recruitment and achieving results crucial to the clinical program's success. They align with NN Korea CDC Project Manager/Clinical Operation Manager, reporting progress and critical issues, and may sometimes interact directly with NN Global Development Trial Managers. The CRA primary tasks in site management will include:Manage clinical trial sites for allocated phase 1-4 clinical trials and non-interventional studies effectively and efficiently, in compliance with NN SOP (standard operating procedures), ICH GCP, GPP (Good Production Practice), KGCP (Korea Good Clinical Practice), and local regulations.Possess good knowledge of trial products an...