• Sr. Clinical Team Manager/Lead- Internal…

    ThermoFisher Scientific (Carlsbad, CA)
    …The Senior Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the ... study protocol) within the time period specified in the contract with the customer. Interprets data on complex issues and makes good business decisions with… more
    ThermoFisher Scientific (01/07/26)
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  • Associate Clinical Project Manager, Sponsor…

    IQVIA (Philadelphia, PA)
    …with the core project team and/or sub-team. + Accountable for assigned portion of clinical studies as per the contract while optimizing speed, quality and cost ... **Position Specifics** This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout.… more
    IQVIA (12/18/25)
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  • Clinical Coordinator

    Suny Polytechnic Institute (Utica, NY)
    …and preceptor information. Accreditation, Evaluation, and Reporting + Collect and maintain clinical data for program evaluation and accreditation (CCNE, NONPF, ... of active agreements. + Serve as the primary contact for clinical partners regarding contract questions or updates. Student Health & Compliance + Verification of… more
    Suny Polytechnic Institute (11/15/25)
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  • Clinical Research Coordinator 2 (Fixed-term…

    Stanford University (Stanford, CA)
    …strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. + Oversee data management for research ... Clinical Research Coordinator 2 (Fixed-term 2 years) **School...care research. The coordinator will be responsible for managing data related to study outcomes, ensuring that all source… more
    Stanford University (01/08/26)
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  • Clinical Research Associate/SR CRA, Field…

    Boehringer Ingelheim (St. Joseph, MO)
    … Research Associate (CRA) conducts in-house and external monitoring to verify that reported data collected in Clinical Lab Studies and Field Trials are accurate, ... sites. + Monitors the progress of in-house studies, field studies, and contract laboratory clinical studies, providing status reports in progression of… more
    Boehringer Ingelheim (01/13/26)
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  • Senior Clinical Trial Manager

    GRAIL (Menlo Park, CA)
    …development of completion guidelines, and other related activities, supporting study requirements and data quality. + Oversees clinical data entry progress ... with site payment terms + Partners with cross functional stakeholders such as Clinical Data Management, Biospecimen Management, Finance, Clinical Compliance,… more
    GRAIL (01/02/26)
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  • SR Scientist, Clinical

    Boehringer Ingelheim (St. Joseph, MO)
    …reflect Boehringer Ingelheim's high regard for our employees. The Senior Scientist, Clinical is responsible for the safety and efficacy in the target species ... line extensions and maintaining existing licensed products. This role provides clinical study design and implementation including resource and budget planning from… more
    Boehringer Ingelheim (12/24/25)
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  • Senior Specialist, Clinical Research…

    Edwards Lifesciences (Kansas City, KS)
    …inspiring journey. **How you'll make an impact:** + Field monitoring of studies and data collection for clinical trials, assess all data documentation, ... your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how… more
    Edwards Lifesciences (11/14/25)
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  • Sr. Manager, Clinical Quality Risk…

    J&J Family of Companies (Raritan, NJ)
    …more at https://www.jnj.com **Job Function:** Quality **Job Sub** **Function:** Clinical Quality **Job Category:** Professional **All Job Posting Locations:** ... Johnson & Johnson is recruiting for a **Sr. Manager, Clinical Quality Risk Management Lead** at a MedTech site...quality risks that could have an impact on trial data integrity, patient rights, safety, or well-being. Throughout the… more
    J&J Family of Companies (01/16/26)
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  • Clinical Trial Specialist

    Actalent (Newark, NJ)
    …sheets. + Verify Scientific Review Board (SRB), Institutional Review Board (IRB), data collection plans, and finance/ contract approvals prior to study ... registering consented research patients with study sponsors and input data into the clinical trials database. +...pediatric studies. Job Type & Location This is a Contract to Hire position based out of Newark, NJ.… more
    Actalent (01/14/26)
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