Clinical Research Coordinator

Clinical Research Coordinators manage the day-to-day operations of clinical trials at investigational sites, coordinating patient enrollment, ensuring protocol compliance, collecting and entering clinical data, managing regulatory documentation, and serving as the liaison between study participants, investigators, and sponsors. They implement Good Clinical Practice (GCP) standards, manage adverse event reporting, and maintain the master file for assigned studies. The pharmaceutical industry's large clinical development pipeline creates sustained demand for experienced coordinators across DACH and MENA.