- University of Colorado (Aurora, CO)
- …in public health or health services research + Experience submitting protocols to an institutional review board ( IRB ) + Experience with reference ... **Qualitative Analyst Research Services Professional Intermediate/ Senior ** **Description**...health services research + Experience submitting protocols to an institutional review board ( IRB… more
- University of Miami (Miami, FL)
- …limited to: Prepare and coordinate the entire process of regulatory document submission to the Institutional Review Board ( IRB ) from study start-up to ... faculty or staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . The University of… more
- Rush University Medical Center (Chicago, IL)
- …of related guidance and their effect on research billing processes. The analyst will provide high-level professional support in the growing efforts to conduct ... analyses with budget overlay in a timely manner. * Review clinical trial protocols and related regulatory documents in...trial under CMS Clinical Trial policy. * Coordinate with IRB staff and the investigator if the IRB… more
- University of Rochester (Rochester, NY)
- …research project working with the PI, the Clinical Trials Office Senior Financial Administrator, Project Coordinators, Industry representatives, ORPA, ORACS, and ... + Post award management activities, including: amendments, contract end dates, review charge reports, categorize services in relation to qualified clinical trials,… more
- Johns Hopkins University (Baltimore, MD)
- …book of business will average $35M annually. This position will provide senior leadership with financial reports and the overall financial management necessary for ... of and interpret monthly and quarterly financial reports for Program and management's review . + Provide ad-hoc reports to clients as requested. + Develop financial… more
- Johns Hopkins University (Washington, DC)
- …and Molecular Radiation Sciences clinical trials under the supervision of the Senior Clinical Research Program Manager at Sibley Memorial Hospital. Major duties are ... is compliant with regulatory and reporting requirements of the IRB and study sponsors including the reporting of adverse...clinical trials group. + Work closely with the Budget Analyst to ensure appropriate research billing is based on… more