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audits. Hybrid work agreement. *Other duties may also be assigned. DESIRED QUALIFICATIONS: Knowledge of the principles of clinical research and federal regulations. Familiarity with IRB guidelines and
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Rutgers ‘commitment to attract exceptional individuals. More information on our program can be found at: https://psych.rutgers.edu/. Rutgers University is an Equal Opportunity Employer. All qualified
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in active clinical trials •Obtaining informed consent •Scheduling and conducting study visits •Preparing IRB Submissions •Acting as the primary contact for study sponsors and participants •Processing
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, including other Harvard Medical School-affiliated hospitals. Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site
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and retirement programs. To learn more about USC benefits, access the "Working at USC" section on the Applicant Portal at https://uscjobs.sc.edu. Position Description Advertised Job Summary Assist in
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collaborative research environment. Ensure compliance with institutional, federal, and state regulations, including IRB, IACUC, IBC, and biosafety requirements. Serve as the primary point of contact for the PI
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accurately and with quality. Adhere to project regulatory protocols (e.g., UNMC, FDA, IRB, HIPAA, lab, sponsor, federal) to meet research participant safety and confidentiality, data quality and security, and
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and IRB amendments, and 4) assist with the establishment and evaluation of a digital technology lending program in through our partners (heads of libraries and community stakeholders), and 5) assist Drs
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Board (IRB) is to support the overall administration of the human research review and approval process, providing high-level support and guidance to investigators and other stakeholders, and streamlining
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for manuscripts and grant proposals. RESEARCH ADMINISTRATION Prepare and process research-related paperwork, including IRB submissions, amendments, and continuing reviews. Monitor compliance with institutional