| The CRA will serve as the primary coordinator of clinical
trial activities to support existing and new pharmacogenomic
products in the AssureRx Health portfolio. The CRA will
establish excellent communication with principal
investigators, research site coordinators, and assistants
while ensuring HIPAA and IRB compliance. The candidate will
assist in all aspects of clinical trial setup, including
protocol development, site evaluation, IRB approval, patient
enrollment, overseeing data collection, and organizing
ongoing study activities. The CRA will use statistical tools
to analyze existing and new clinical data, and prepare
summaries and reports of these findings. |
