• Senior Specialist, Clinical Research

    Edwards Lifesciences (Kansas City, KS)
    …+ Bachelor's Degree and a minimum of 5 years of work experience in clinical research monitoring , with a strong focus on quality assurance, quality control, and ... part of our inspiring journey. **How you'll make an impact:** + Field monitoring of studies and data collection for clinical trials, assess all data documentation,… more
    Edwards Lifesciences (11/14/25)
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  • Director, Office Of Research And Program…

    City of New York (New York, NY)
    …plans/support, domestic violence assistance, child support enforcement, etc. Office of Research and Program Monitoring (ORPM) functions as Family Independence ... and initiative, is responsible for the oversight of the Office of Research and Program Monitoring with a particular focus on organizational research and… more
    City of New York (12/21/25)
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  • Research Monitoring Specialist

    Arkansas Children's (Little Rock, AR)
    …description for details. **Time Type:** Full time **Department:** CC033007 Research Integrity **Summary:** **Additional Information:** Responsible for monitoring ... **Recommended Certifications:** **Description** 1. Develop, implement, and maintain a monitoring program and tools for human research ....a monitoring program and tools for human research . 2. Obtain documents and assure the files are… more
    Arkansas Children's (12/30/25)
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  • Specialist, Clinical Research

    Edwards Lifesciences (St. Paul, MN)
    …of our inspiring journey. **How you will make an impact:** + Field monitoring of studies and data collection for clinical trials, assessing all data documentation, ... subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good Clinical… more
    Edwards Lifesciences (01/13/26)
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  • Traffic Monitoring Supervisor…

    State of Minnesota (St. Paul, MN)
    **Working Title: Traffic Monitoring Supervisor** **Job Class: Research Analyst Supervisor Senior** **Agency: Transportation Dept** + **Job ID** : 91284 + ... with their supervisor. This position manages Minnesota's statewide Traffic Monitoring Program, ensuring accurate traffic data collection, analysis, and reporting… more
    State of Minnesota (01/14/26)
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  • Research Compliance Monitor, IRB

    Wayne State University (Detroit, MI)
    …prepare students for success in a global society. Position Purpose: Conduct post-approval research monitoring visits to observe and document research conduct ... and regulatory compliance. Submit monitoring reports to the Human Research Protection Program Administration and to the Institutional Review Boards for… more
    Wayne State University (01/13/26)
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  • Senior Clinical Research Associate/Clinical…

    Parexel (Austin, TX)
    …Specialist, Clinical Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience: Minimum 3 years relevant ... experience in clinical research site monitoring (preferably 2 years in Oncology) in a CRO or pharma organization + Preferred therapeutic experience in Oncology +… more
    Parexel (12/07/25)
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  • Investment Manager - Portfolio Research

    PNC (Pittsburgh, PA)
    …STEM OPT for this position. **Job Description** + Performs analysis, due diligence research , monitoring and analytical activities for a variety of investment ... an opportunity to contribute to the company's success. As an Investment Manager - Portfolio Research Associate III, you may be based in a remote location. This is a… more
    PNC (01/13/26)
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  • Wildlife Research Intern

    State of Minnesota (Madelia, MN)
    …learn about and help implement DNR/Division of Fish and Wildlife (FAW) wildlife research and population monitoring projects, primarily upland game (eg, pheasants ... through mid- to late August. Current active upland game and ungulate research and monitoring projects that the intern will be involved in assisting with include:… more
    State of Minnesota (01/14/26)
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  • Sr. Clinical Research Associate - Oncology…

    Parexel (Charleston, WV)
    …+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) + Preferred therapeutic ... The Senior Clinical Research Associate (Sr. CRA) is responsible for the...(Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites… more
    Parexel (12/11/25)
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