• Clinical Research Specialist II…

    Cedars-Sinai (Los Angeles, CA)
    …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and ... and collaborative, multi-site clinical research. The CCC Clinical Research Specialist II will serve in a cross-functional...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
    Cedars-Sinai (06/25/25)
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  • Clinical Research Data Specialist II…

    Cedars-Sinai (Los Angeles, CA)
    …and local agencies, including the Food and Drug Administration (FDA) and local Institutional Review Board . Primary Duties and Responsibilities: + ... ready to be a part of breakthrough research?** The Clinical Research Data Specialist II independently manages data for assigned research studies, demonstrating a… more
    Cedars-Sinai (07/10/25)
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  • Research Nurse Specialist II…

    Vanderbilt University Medical Center (Nashville, TN)
    …Research Staff Council monthly meetings. + Attends in-services advertised by the Institutional Review Board , Research Support Services, professional ... and supervision of the Principal Investigator, the Research Nurse Specialist II (RNS II ) is...processes new IRB research proposals, amendments, continuing review applications and adverse events according to institutional… more
    Vanderbilt University Medical Center (07/26/25)
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  • Research Grant Specialist II…

    Cedars-Sinai (Los Angeles, CA)
    …local agency requirements including the Food and Drug Administration (FDA) and local Institutional Review Board . **Primary Job Duties and Responsibilities:** ... care the most. **Req ID** : 11255 **Working Title** : Research Grant Specialist II - Department of Medicine - Hybrid **Department** : Medicine - Admin **Business… more
    Cedars-Sinai (08/02/25)
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  • Clinical Trials Specialist II (ETS)…

    Emory Healthcare/Emory University (Flowery Branch, GA)
    …and monitors practices to ensure regulatory documentation involving clinical trials complies with Institutional Review Board ( IRB ) policies and ... of our academic community. **Description** JOB DESCRIPTION: The Regulatory Specialist II is an intermediate level position...to various review committees, including internal scientific review boards, the IRB and sponsoring entities.… more
    Emory Healthcare/Emory University (08/21/25)
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  • Regulatory Specialist - CRI

    Methodist Health System (Dallas, TX)
    …the IRB . * Create and/or adapt clinical trial informed consent documents for Institutional Review Board ( IRB ) submission. * Maintain regulatory ... Shift :** **Job Description :** Your Job: The Regulatory Specialist will perform expertise in the regulatory component of...research trials to include, but not limited to; Phase II and IV clinical, investigator initiated trials (IITs), and… more
    Methodist Health System (08/08/25)
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  • Research Support Specialist

    Stony Brook University (Stony Brook, NY)
    …reagents in the lab + Maintain study protocol documents and ensure compliance with all Institutional Review Board ( IRB ) and Safety policies. + Other ... Research Support Specialist **Required Qualifications (as evidenced by an attached resume):** Bachelor's Degree (foreign equivalent or higher) in Biology or a… more
    Stony Brook University (08/23/25)
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  • Research Assistant II - Biorepository

    Baylor Scott & White Health (Temple, TX)
    …certification optional, but appreciated. + Will assist in development and maintenance of IRB approval in the role of regulatory specialist . + May obtain ... Testing program. + Communicates with IRB and submits IRB documentation as needed (ie, continuing review , KSP) + Any other tasks as assigned by management… more
    Baylor Scott & White Health (07/15/25)
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  • Human Sub Research Spec II

    University of Rochester (Rochester, NY)
    …the research team. May provide mentorship to Human Subject Research Specialist I. **ESSENTIAL FUNCTIONS** **Study Visits:** Recruits, consents, schedules, and ... and communicating as needed. **Mentoring:** Mentors and trains Human Subject Research Specialist I (HSRS I) on activities related to conducting human subject… more
    University of Rochester (08/07/25)
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  • Clinical Research Coordinator II

    Hartford HealthCare (Hartford, CT)
    …portfolio of cancer research studies. In compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and ... monitoring of protocol for compliance and patient safety; source document review ; data entry; sponsor monitoring. * Interact/collaborate with all physicians, other… more
    Hartford HealthCare (06/23/25)
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