Description
SGS is hiring a clinical studies coordinator to manage and support daily clinical study activities in compliance with protocols, GCP, SOPs, and applicable regulations. The role involves preparing and maintaining study documentation, coordinating subjects and clinic setup, assisting with IRB/regulatory submissions, responding to QA and statistics queries, training staff, and providing strong client and panelist service. A bachelor’s degree in science or a related field and at least two years of relevant experience are required, with CCRC/CCRA certification as a strong plus.
