• Director, Clinical Data Management…

    Regeneron Pharmaceuticals (Warren, NJ)
    …biotech, or clinical research organization. + Knowledge of clinical data management principles, technologies, data extraction, transformation, and ... The Director of Clinical Data Management Reporting will provide...internal audits and health authority inquiries. + Establish and monitor KPIs to track performance, conformance with programming standards,… more
    Regeneron Pharmaceuticals (01/08/26)
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  • Data Scientist II for Published…

    AbbVie (South San Francisco, CA)
    …years), or Ph.D. (0-2 years) in life sciences, medicine, pharmacy, bioinformatics, biomedical/ clinical data science, or related field + Solid scientific domain ... resources and internal knowledge. This includes literature, patent, conference, news, clinical trial, and competitive intelligence data such as competitor… more
    AbbVie (01/10/26)
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  • Post-Approval Compliance Monitor

    Alaka'ina Foundation Family of Companies (Silver Spring, MD)
    …training, as needed/requested. DESCRIPTION OF RESPONSIBILITIES: The WRAIR-based clinical research scientific monitoring services (Post-Approval Compliance ... EXPERIENCE: + Minimum three (3) years experience as a Clinical Trial Monitor + Knowledge and experience... + Knowledge and experience in the areas of clinical research and regulatory affairs as related… more
    Alaka'ina Foundation Family of Companies (01/15/26)
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  • Asst Dir, Clinical Optimization…

    WMCHealth (Valhalla, NY)
    Asst Dir, Clinical Optimization & Data Analytics Company: WMC Advanced Physician Services PC City/State: Valhalla, NY Category: Executive/Management Department: ... link Job Details: Job Summary: The Assistant Director of Clinical Optimization and Data Analytics for Infection...external reporting databases + Developing tools and processes to monitor and analyze data accuracy + Building… more
    WMCHealth (11/01/25)
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  • Phlebotomist and Abstinence Monitor

    University of Colorado (Aurora, CO)
    …**Preferred Qualifications:** + One (1) year of phlebotomy experience in a professional, clinical or research setting. + Experience working with patients who ... **Phlebotomist and Abstinence Monitor ** **Description** **University of Colorado Anschutz Medical Campus**...**School of Medicine | Department of Psychiatry | Addiction Research & Treatment Services (ARTS) | Adult Outpatient Program**… more
    University of Colorado (12/18/25)
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  • Research Coordinator 1 (NE S UAW…

    University of Washington (Seattle, WA)
    …and apply study protocols. * Monitor study eligibility. * Collect and record clinical data from a combination of electronic medical record systems review and ... presented at conferences or published in scientific journals. * Monitor several studies and report findings to principal investigators,... environment, clinical research , laboratory research , project coordination, research data more
    University of Washington (01/14/26)
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  • Research Nurse (DOM Bay Rheumatology)…

    Johns Hopkins University (Baltimore, MD)
    …_Data Collection and Documentation_ + Collect, abstract, and enter demographic and clinical data into Epic SmartForms, flowsheets, and registry databases. + ... reviewers as required. _Occasional Trial Support_ + Provide backup support to clinical research coordinators for trial-related tasks, such as patient screening… more
    Johns Hopkins University (11/08/25)
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  • Research Program Coordinator in Precision…

    Stanford University (Stanford, CA)
    …of biotype-guided clinical precision mental health studies and any other assigned clinical research groups within the Center. The Research Program ... the Center, and utilize this knowledge to conduct impactful clinical research with a focus on high...Develop and manage systems to organize, collect, report, and monitor data collection. + Extract, analyze, and… more
    Stanford University (12/16/25)
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  • Research Nurse

    Catholic Health Services (West Islip, NY)
    …+ Collects and submits data to sponsors and database as required; ensures that clinical research data is accurate, legible, timely and in compliance with ... records, interviews, questionnaires, diagnostic tests and other sources. Enters data into relevant EDC in a timely manner +...complete, accurate, and readily available for clinical research audits or study sponsor monitor visits,i.e.:… more
    Catholic Health Services (01/02/26)
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  • Research Coordinator - RN

    University of Rochester (Rochester, NY)
    …to assess subject eligibility, clinical status, and adverse reactions. + Monitor research participants for local and systemic reactions and document adverse ... and well-being of research participants while maintaining high standards of data integrity and regulatory compliance. The Clinical Trials Research more
    University of Rochester (12/05/25)
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