Responsible for the day-to-day management and operations of multiple large scale clinical research projects under the guidance of principal investigators from the Department of Surgery and Perioperative Care. Execute clinical research protocols including patient recruitment, obtaining informed consent, completing study related procedures, accounting for study drug and investigational devices, and documenting compliance.Responsible for clinical tasks including lab preparation of specimens, vital signs, ECGs and administration of questionnaires. .Manage logistics and permissions associated with hospital based clinical research. Develop and create systems for analysis and data collection. Develop coverage analysis and work with pre-and post-award finance departments to coordinate contracting, invoicing and purchasing. Responsible for clinical communications with sponsors, CROS, central and local IRBs, vendors and investigators.Develop research protocols and grant proposals, informed consent forms, questionnaires, recruitment tools and other forms of documentation.Maintain ethical approval for studies, from initial study approval through study amendments, annual continuations and terminations. Maintain all CRF and source documents according to FDA and IRB guidelines. Ensure all study personnel have appropriate training in research ethics (e.g. CITI, GCP).Coordinate interdisciplinary teams of investigators, research assistants, clinical staff members and others contributing to executing elements of research being conducted within Dell Medical School and affiliates. Ensure that all investigators and staff executing research are appropriately trained in procedures.Other related duties as assigned.