• Research Reliance Director

    University of Rochester (Albany, NY)
    …Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 100045 Office for Human Subject Prot Work Shift: UR - Day (United States of America) ... General Purpose Directs all aspects of the Office for Human Subject Protection (OHSP) research reliance program, which requires oversight and… more
    University of Rochester (05/24/25)
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  • Clinical Science Professional (Open Rank:…

    University of Colorado (Aurora, CO)
    …regulatory compliance, sponsor communication and post and pre award management, human subject compliance, research animal management, research laboratory ... of larger project from initiation to close. + Obtain study subject 's medical history and current medication information, reviews research protocol… more
    University of Colorado (03/08/25)
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  • Research Ed & Training Dir

    University of Rochester (Rochester, NY)
    …Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 100045 Office for Human Subject Prot Work Shift: UR - Day (United States of America) ... **Responsibilities:** GENERAL SUMMARY Directs all aspects of the Office for Human Subject Protection (OHSP) research education and training program to promote… more
    University of Rochester (05/11/25)
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  • Clinical Sciences Professional (Open Rank)-…

    University of Colorado (Aurora, CO)
    …regulatory compliance, sponsor communication and post and pre award management, human subject compliance, research animal management, research laboratory ... functions which may include patient-oriented research or research conducted with human subjects. Patient-oriented research includes mechanisms of human disease,… more
    University of Colorado (03/08/25)
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  • Clinical Sciences Professional (Open Rank…

    University of Colorado (Aurora, CO)
    …with other research personnel and groups + Maintain study-specific certifications, human subject protection training, computer training, and other ... and their offspring. In our group, we study both investigator and industry-initiated human subject trials. The lab is seeking to recruit an individual with prior… more
    University of Colorado (04/30/25)
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  • Clinical Research Coord Assoc / Tech / Asst - Term…

    University of Michigan (Ann Arbor, MI)
    …Administration, Social Work, Psychology, Epidemiology, Foreign MD. + Minimum 3 years of human subject experience (clinical, lab or health regulations) such as ... management activities. + Performs study procedures with minimal supervision. + Triages subject issues appropriately. + Schedules and runs study visits with complex… more
    University of Michigan (05/14/25)
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  • Clinical Research Coordinator A (Department…

    University of Pennsylvania (Philadelphia, PA)
    …federal regulations and guidance documents for the conduct of clinical studies involving human subject and their protection. + Assure compliance with the ... binders through subject study completion. + Coordinate and conduct human subject clinical study including: subject recruitment; visit scheduling and… more
    University of Pennsylvania (05/10/25)
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  • Sr. Compliance Monitoring Specialist

    Johns Hopkins University (Fort Defiance, AZ)
    …aspects of pertinent tribal government regulations and institutional policies pertaining to human subject 's research and related matters. + Review applications ... of customer service. + Perform other duties as required related to human subject 's research practice, as requested by the Principal Investigators and Directors.… more
    Johns Hopkins University (04/11/25)
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  • IRB Administrator I

    Tufts Medicine (Boston, MA)
    …IRB reviewer(s). 16. Provides ongoing consultation to investigators on issues pertaining to human subject protections and the IRB review process. 17. Manages and ... coordinates continuing education program about human subject protections for IRB members, IRB staff and investigators. 18. Presents education sessions and… more
    Tufts Medicine (05/31/25)
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  • Senior Director, Clinical Research (IRB)

    Northwell Health (New Hyde Park, NY)
    …and consent documents in accordance with applicable regulations and reporting requirements for human subject research. 7. Maintains official IRB records, eg IRB ... a liaison to federal and NY State agencies and committees, which regulate human subject research, as required. 4. Team Management: 1. Oversees and evaluates the… more
    Northwell Health (05/24/25)
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