• Nurse Navigator ( Research )

    Saint Francis Health System (Tulsa, OK)
    …( Research ) ensures the clinical assessment and clinical care provided to research subjects meets all regulatory requirements and research protocol. ... This position understands the disease process and research treatment. This role provides education and coordination to research participant consumers (patients,… more
    Saint Francis Health System (06/27/25)
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  • Clinical Research Specialist II - Clinical…

    Cedars-Sinai (Los Angeles, CA)
    …+ Bachelor's Degree required. + 5 years of experience in clinical research , regulatory , or data coordination required. + Experience with investigator-initiated ... and expertise for investigator-initiated trials (IITs) and collaborative, multi-site clinical research . The CCC Clinical Research Specialist II will serve… more
    Cedars-Sinai (06/25/25)
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  • Clinical Research Associate,…

    IQVIA (Durham, NC)
    …degree. Req * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice (GCP) and International ... IQVIA is hiring a Clinical Research Associate with on-site monitoring experience in GLP-1/Obesity/Diabetes...visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International… more
    IQVIA (07/04/25)
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  • Adjunct Instructors - Regulatory Affairs…

    Minnesota State (St. Cloud, MN)
    …Bachelor's Degree + Minimum of ten years of applicable industry experience in Regulatory Affairs, Clinical Research , Quality or Reimbursement + Advanced degree ... Closing Date (if designated).** **Working Title:** Adjunct Instructors - Regulatory Affairs and Services **Institution:** St. Cloud State University **Classification… more
    Minnesota State (06/03/25)
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  • Clinical Research Coordinator, On-Site

    IQVIA (Metairie, LA)
    …assigned **Qualifications** + Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines + Clinical Research Coordinator experience within a ... team-oriented setting and is eager to make a meaningful impact through clinical research . **Overview:** This individual will play a key role in assisting in the… more
    IQVIA (08/09/25)
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  • Senior Clinical Research Coordinator…

    UCLA Health (Los Angeles, CA)
    …preparation of clinical trial budgets. + Advance knowledge of the clinical research regulatory framework and institutional requirements. All Required + Ability ... is seeking to hire a full time Senior Clinical Research Coordinator. In this role you will play a...critical role in the overall operational management of clinical research / trial / study activities from design, set… more
    UCLA Health (08/01/25)
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  • (Senior) Clinical Research Associate…

    IQVIA (Carlsbad, CA)
    …degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and International ... and close-out visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on… more
    IQVIA (07/14/25)
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  • Clinical Research Associate, Sponsor…

    IQVIA (Parsippany, NJ)
    …customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree in ... - escalating quality issues as appropriate + Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query… more
    IQVIA (07/31/25)
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  • Clinical Research Associate - Clinical…

    Queen's Health System (Honolulu, HI)
    …in a research setting. * Experience to demonstrate knowledge of research regulatory processes (human subject protection, biological safety, conflict of ... RESPONSIBILITIES I. JOB SUMMARY/RESPONSIBILITIES: * Conducts clinical research studies under the immediate direction of assigned Principal Investigator. * Assists… more
    Queen's Health System (07/03/25)
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  • Clinical Research Associate, Full Service

    IQVIA (Overland Park, KS)
    …customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.You should have: + A Bachelor's degree in a ... quality issues as appropriate + Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and...you want to make an impact in the global research market, where we are working to make a… more
    IQVIA (06/27/25)
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