- Emory Healthcare/Emory University (Atlanta, GA)
- …investigational or marketed drugs. + Serves as a representative of Emory University on the Institutional Review Board ( IRB ) to assist in protocol ... **Discover Your Career at Emory University** Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate… more
- General Dynamics Information Technology (Portsmouth, VA)
- …at the Naval Medical Center Portsmouth (NMCP). The CRC is responsible for providing research coordination support for IRB - and IACUC -approved human and animal ... by the government entity may be required for safety reasons. + Coordinate research activities of assigned IRB and IACUC-approved study protocols, such as… more
- Beth Israel Lahey Health (Boston, MA)
- …for participation in multiple clinical trials, ensuring compliance with federal , state and institutional guidelines. Financial responsibilities including ... submits protocols, amendments, notices, suspensions and terminations to the IRB for review and approval. (essential) +...with patients. Revises protocol consent form to comply with federal , state and IRB guidelines. (essential) +… more
- University of Utah (Salt Lake City, UT)
- … Research Suite for use in Conflict of Interest ( COI ) and Institutional Review Board ( IRB ). The software engineer will work primarily with the ... Research . ORIS primarily supports Pre-Award and Post-Award grant management, the Institutional Review Board , Conflict of Interest, and other… more
- University of Pennsylvania (Philadelphia, PA)
- …visits with CROs, the FDA and other entities. + Correspond regularly with the Institutional Review Board and other regulatory agencies, including preparation ... employer in Philadelphia, is a world-renowned leader in education, research , and innovation. This historic, Ivy League school consistently...FDA and other entities. + Correspond regularly with the Institutional Review Board and other… more
- University of Pennsylvania (Philadelphia, PA)
- …documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports. ... documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.… more
- Dana-Farber Cancer Institute (Boston, MA)
- …applications, amendments, continuing reviews, and informed consent documents for SRC and IRB review and approval. + Prepares and submits regulatory documentation ... groups, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizations. Works interactively… more
- Texas Tech University Health Sciences Center - El Paso (El Paso, TX)
- …well as preparing reports and documentation for stakeholders and regulatory bodies like the Institutional Review Board ( IRB ). **Requisition ID:** 43148BR ... Sci Ctr El Paso **Position Description:** Supports the Director in managing research projects from start to finish, including planning, data collection and analysis… more
- University of Utah (Salt Lake City, UT)
- …notifications and submits amended protocols, summaries, and consents to the Institutional Review Board ( IRB ). 6. Submits study renewal applications ... process improvements. 10. Maintains current knowledge of federal and institutional guidelines and requirements governing research . 11. Maintains regulatory… more
- Cedars-Sinai (Los Angeles, CA)
- …agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices using Good Clinical Practice ... **Job Description** The Clinical Research Data Specialist I manages the data for...including the Food and Drug Administration (FDA) and local Institutional Review Board . ESSENTIAL JOB… more