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Master's degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.
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Represent Precision Medicine function at advisory boards and health authority interactions to advance translational research and clinical biomarker objectives for the program. Author and review Precision Medicine related sections in clinical study / regulatory documents (i.e. INDs, IBs, trial protocols/ops manuals, ICFs, IRB responses, HA Briefing Books, CSRs, etc.
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The research assistant's primary responsibilities will be writing IRB amendments, primary data collection, development of study materials and supplies, curriculum delivery, communications with participants at the Native American Youth Camp, and results preparation for presentations and manuscripts.
$47,356 - $59,195 a yearExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Facilitates preparation of IRB protocol submissions and informed consent forms. Responsible for completing and maintaining all study documents, in compliance with IRB, Cooper Health System, sponsor and FDA requirements.
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Required Education and Experience:Bachelor's degree in life science, health professions or related field and four years of directly related clinical research coordinator experience. Primary responsibilities include the coordination of study enrollment; oversight of study protocols; and submission of research activities per IRB regulations.
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Assist Regulatory specialist in preparing and maintaining, IRB (eResearch) applications including new applications, scheduled continuing reviews, amendments, adverse event reporting (events that either occurs in UM research subjects or subjects from other centers in multi-site studies) and other reportable information and occurrences.
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Works with the Baptist Health Sciences University (BHSU), Office of Finance, and Baptist Memorial Health Care Corporation (BMHCC) to develop and refine procedures and/or polices to support proposal submission, compliance, budgeting, and other relevant processes with adherence to applicable BHSU, state, and federal guidelines.
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The Senior Research Specialist will be expected to accompany participants to the neuroimaging locations and take part in general project management, including IRB-related procedures, and oversee quality control processes.
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The position bridges a wide-gap-real and perceived- among tribal public health system stakeholders (e.g., tribal nations, tribal/urban communities, academia, non-profit organizations, and government agencies) with respect to health and health - related planning, evaluation, and research.
$4,736 - $5,834 a monthFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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May participate in the Health Authority (HA) and IEC/IRB submission and notification processes as required/appropriate. Janssen Research & Development, L.L.C., a division of Johnson & Johnson's Family of Companies is recruiting for a Senior Site Manager, Global Clinical Operations - Oncology, to be remote in the Southeast Region ( DC, VA, MD, NC, SC, GA, FL, WV ) of the United States.
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Primary responsibilities of this position include: 1) recruitment of research participants 2) collection of qualitative and quantitative research data; 3) preparing IRB protocols; 4) maintain compliance with IRB and study training and documentation requirements; 5) management, tracking, and limited analysis of study data; 6) participating in preparation of presentations and manuscripts; and 7) performing miscellaneous related tasks as required.
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Position Summary: The Clinical Research Coordinator III, as a certified research professional, handles clinical trial administration for all protocol phases for the Leukemia and Lymphoma Disease department.
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The Research Compliance Officer will provide support and direction for the NYSPI research enterprise by functioning as an independent monitor of NYSPI's plan for comprehensive redesign of its Human Research Protections Program and IRB. The Compliance Officer will partner with NYSPI's Director of Research in HRPP and IRB oversight activities but will report directly to NYSPI's external Human Subjects Research Governance Board.
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Prepares and submits regulatory documents for all submissions to St. Luke's Research and the IRB of record on behalf of investigators. St. Luke’s Health System in Boise, ID is seeking a Research Regulatory Coord 2 to join our Clinic Administration Oncology team.
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QualificationsPreferred qualifications and skills:•PhD (or comparable terminal degree) in Health Services Research, Epidemiology, or a closely related field. Consult and assist faculty and research fellows on patient-reported outcomes-related project design, grant applications, study protocols, manuscripts, or IRB submissions.
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