Campus Pride Jobs

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 screening, recruitment, obtaining informed consent, completing study related procedures, accounting for study drug and investigational devices, and documenting compliance.Responsible for clinical tasks (examples include lab preparation of specimens, vital signs, ECGs) and administration of questionnaires.Manage logistics associated with clinic- and hospital-based clinical research for industry-sponsored projects.Manage data collection.Work with pre-and post-award contacts to coordinate contracting, invoicing and purchasing.Responsible for communications with sponsors, clinical research organizations (CROs), central and local IRBs, vendors, participants, and investigators.Assist faculty in developing 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 case report forms (CRF) and source documents according to FDA and IRB guidelines.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 research human subjects research and procedures.Other related duties as assigned.