• Coordinates and implements SC system-wide processes and initiatives to standardize clinical research operations • Facilitates research activities through collaborative, timely communications with SHC sites and external entities • Maintains and assists with the system wide use and daily operations of the clinical research management system • Accountable for the initiation and maintenance of all Human Subjects and Regulatory documents necessary for submission to SC’s centralized Institutional Review Board • Works with study sponsors and various agencies to obtain initial and continued approval of all clinical trials/clinical research protocols • Demonstrates knowledge of ethical standards set forth by the Belmont Report, the Nuremberg Code and the International Conference of Harmonization GCP standards • Supports coordination of system-wide genomics clinical research activities, including protocol development and executions