JOB SUMMARY:Under general supervision of the Associate Director â“ Clinical Trials Office (CTO), the Clinical Regulatory Manager ensures the CTO complies with federal and state regulations pertaining to human subject research as well as internal Saint Louis University policies and procedures. The Clinical Regulatory Manager is responsible for assisting in the IRB review completion and submission. Participates in the monitoring of clinical trials. Ensures compliance with protocol and overall clinical objectives. Knowledge of FDA regulatory requirements is required. May require ACRP or SOCRA Clinical Research Professional exam completion.PRIMARY JOB RESPONSIBILITIES:Responsible for completion and submission of the CTOs re