• Clinical Site Monitor

    University of Utah (Salt Lake City, UT)
    Details **Open Date** 12/04/2025 **Requisition Number** PRN43738B **Job Title** PS Clinical Site Monitor **Working Title** Clinical Site Monitor ... object to vaccinations. Preferences include credentialing as a Certified Clinical Research Associate ( CCRA...Professional ( CCRP ). Prior experience as an industry CRA or Monitor is also preferred. Hiring… more
    University of Utah (01/07/26)
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  • Sr. Clinical Research

    Parexel (Charleston, WV)
    The Senior Clinical Research Associate (Sr. CRA ) is responsible for the site management, site monitoring and close-out of assigned clinical ... needed + May undertake the responsibilities of an unblinded monitor where appropriate ** Clinical /Scientific and Site...+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably… more
    Parexel (12/11/25)
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  • Senior Clinical Research

    Parexel (Austin, TX)
    **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA ) is responsible for the site management, site monitoring and close-out of ... Clinical Practices (GCP), and sponsor standards. The Sr. CRA is accountable for site management and...+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably… more
    Parexel (12/07/25)
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  • Clinical Research Associate 3

    Grifols Shared Services North America, Inc (Research Triangle Park, NC)
    …market innovative medicines, solutions and services in more than 110 countries and regions. The Clinical Research Associate assists in the management of the ... a life science field preferred. + Typically requires 5 years of experience in clinical research , including a minimum of 2 years field monitoring experience and… more
    Grifols Shared Services North America, Inc (11/08/25)
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  • Clinical Research Associate

    IQVIA (Houston, TX)
    …help bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate ( CRA ) to join our team ... 2 with a minimum of 1 year of on- site monitoring and will also consider CRA ...will directly contribute to the integrity and quality of clinical research data. **Key Responsibilities** + Conduct… more
    IQVIA (01/05/26)
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  • Senior Clinical Research

    BeOne Medicines (Emeryville, CA)
    **General Description:** The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ... with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site ...audit/inspection findings to resolution as it related to involved CRA staff. * Assist with other assigned clinical more
    BeOne Medicines (12/19/25)
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  • Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    Job Summary: A Clinical Research Associate I will have a detailed understanding of each study protocol and background knowledge of the study medication and ... patients closely for any associated adverse events. + Maintain clinical research records; maintain files of approval...Interacts with investigators and their staff to facilitate and monitor the conduct of multidepartment clinical studies.… more
    SUNY Upstate Medical University (12/01/25)
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  • Lead Clinical Research

    University of Southern California (San Diego, CA)
    …provide guidance to clinical monitors for sponsor and investigator initiated clinical research studies. Assists in administration of the consent process, and ... The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is...Team at study specific meetings. Provide study updates on Clinical Monitoring team metrics, site escalations, and… more
    University of Southern California (01/08/26)
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  • Clinical Research Monitor

    General Dynamics Information Technology (Fort Detrick, MD)
    …**US Citizenship Required:** Yes **Job Description:** **GDIT's Military Health team is hiring a Clinical Research Monitor to support the Office of Regulated ... **HOW YOU WILL MAKE AN IMPACT:** **Develop a Clinical Monitoring Plan and monitor single site and multicenter clinical studies both inside and outside… more
    General Dynamics Information Technology (11/19/25)
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  • Clinical Development Medical,…

    Pfizer (Pearl River, NY)
    …analysis and reporting. + Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts with ... enable quality, compliance and patient safety at the trial, site and patient level. + Ensures development of and...feasibility. **Support study team** + With supervision of medical monitor (Director/Sr Director) provides clinical input to… more
    Pfizer (01/11/26)
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