• Clinical Trial Coordinator

    Actalent (Somerville, NJ)
    … is responsible for coordinating the initiation and activation of all new clinical trial protocols. This includes verifying approvals from the Scientific Review ... Job Title: Clinical Research Coordinator Job Description The...Responsibilities + Coordinate the initiation and activation of new clinical trial protocols. + Verify approvals from… more
    Actalent (07/12/25)
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  • Senior Clinical Research Coordinator

    Vitalief (New Brunswick, NJ)
    …that ultimately benefit patients.​ We are seeking a talented and enthusiastic Senior Clinical Research Coordinator to join our exceptional team (as full-time, ... documents, study documents and forms. + Schedules and conducts trial visits by informing patients and coordinating procedures per...of experience in clinical research as a Clinical Research Coordinator , with experience in patient… more
    Vitalief (07/12/25)
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  • Senior Clinical Research Coordinator

    Vitalief (New Brunswick, NJ)
    …years of experience in clinical research as a Clinical Research Coordinator , with experience in patient recruiting/pre-screening/consenting/retention; ... of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise...surgeons at the site to review surgical schedule for trial participants to ensure there is sufficient coverage -… more
    Vitalief (06/05/25)
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  • Staff Psychologist

    Veterans Affairs, Veterans Health Administration (Lyons, NJ)
    …a Allied Health Professional Duties: The Psychologist Oversees the day-to-day clinical and administrative operations of the SUD-RRTP. The SUD-RRTP provides ... with all regulations of the Veterans Health Administration and ensures that Clinical documentation complies with VANJ policies and current standards of practice for… more
    Veterans Affairs, Veterans Health Administration (07/11/25)
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  • Associate Manager, Compliance, Training…

    Sumitomo Pharma (Trenton, NJ)
    …MHRA, and PMDA regulatory frameworks. + Proficient in end-to-end case management of clinical trial and post-market ICSRs. + Experienced in supporting partner ... interactions with archiving vendors as applicable. Serves as records Information Management coordinator + Works with the PV person(s) for compliance to address… more
    Sumitomo Pharma (05/16/25)
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