Description
The Data Coordinator supports a Study Coordinator in clinical trials by obtaining source documentation, assisting with case report form completion and query resolution, tracking serious adverse events, maintaining patient visit spreadsheets, archiving study files, and supporting procedural projects. The role requires knowledge of scientific, medical, regulatory, GCP, and GMP terminology; attention to detail; and excellent English communication skills. A bachelor's degree and healthcare, clinical-trial, or pharmaceutical experience are preferred.
