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extensive interaction wth the Internal Review Board (IRB), study sponsors, and investigators. Job Description Primary Duties & Responsibilities: Responsible for the management of the Division of Clinical
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preparation of submission forms. Instructions to Applicants: For full consideration, applicants must apply for the IRB Compliance Specialist at https://jobs.gmu.edu/. Complete and submit the online application
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Posting Details Position Information Job Title Senior IRB Analyst Position Number 500684 Vacancy Open to All Candidates Department AAH REDE Institutional Review Board Department Homepage https
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Posting Details I. DEPARTMENT INFORMATION Job Description Summary: The Research Associate is expected to have some experience in clinical research: submitting IRB protocols and consent forms
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policies as they relate to assigned research protocols. Under supervision of MnDRIVE and Psychiatry Regulatory Specialist, create and manage regulatory files for new studies. Completes IRB and other required
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of investigator-initiated and industry-sponsored clinical trials. Assist with study start-up activities, including regulatory submissions, IRB documentation, study activation, and investigator files
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minimum of 16.0 hours per week must be in-person at the IRB office on University of Utah campus. In-office requirements are subject to change per University and department policy. VP Area President
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, including coordination, organization and maintenance of all documentation required by Sponsor or CRO as well as working with partnering institutions on managing invoicing, and IRB paperwork under limited
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protocols. Under supervision of MnDRIVE and Psychiatry Regulatory Specialist, creates regulatory files for new studies. Completes IRB and other required review committee applications on assigned protocols
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Location Lexington, KY Grade Level 46 Salary Range $53,061-87,526/year Type of Position Staff Position Time Status Full-Time Required Education PhD Click here for more information about equivalencies: https