• IRB Coordinator Consultant

    Vitalief (Livingston, NJ)
    …will support a leading hospital research center in Livingston, NJ, administering and overseeing Institutional Review Board ( IRB ) activities to ensure ... grow sustainably. The Role We are seeking an experienced IRB Coordinator Consultant to join the Vitalief...human subjects research. This role supports investigators, staff, and IRB members in the preparation, review , and… more
    Vitalief (10/05/25)
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  • Clinical Research Coordinator

    Vitalief (New Brunswick, NJ)
    …Practice (GCP) guidelines. + Experience in preparation of documents for submission to the Institutional Review Board ( IRB ), continuing reviews, and ... of experience in Clinical Research as a Clinical Research Coordinator , with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance… more
    Vitalief (07/15/25)
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  • Research Coordinator

    RWJBarnabas Health (Livingston, NJ)
    …Location: 94 Old Short Hills Road, Livingston, NJ 07039 Job Title: Research Coordinator Location: Cooperman Barnabas Medical Ctr Department Name: MS Research Req #: ... educational background, skills and professional experience. Job Overview: The Research Coordinator will coordinate all clinical activities of research for the MS… more
    RWJBarnabas Health (09/19/25)
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  • Senior Clinical Research Coordinator

    Vitalief (New Brunswick, NJ)
    …patients.​ We are seeking a talented and enthusiastic Senior Clinical Research Coordinator to join our exceptional team (as full-time, fully benefited Vitalief ... study budget, startup meeting preparation, training staff, and preparation of IRB applications and preparation of regulatory documents, study documents and forms.… more
    Vitalief (07/12/25)
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  • Clinical Trial Specialist Consultant

    Actalent (Long Branch, NJ)
    …will involve verifying approvals from the Scientific Review Board (SRB), Institutional Review Board ( IRB ), Human Research Oversight Committee ... clinical trial protocols. + Verify Scientific Review Board , Institutional Review Board...+ 1-3 years of experience as a Clinical Research Coordinator . + Experience in clinical research and oncology. +… more
    Actalent (10/02/25)
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