• Clinical Research Coordinator B/C

    University of Pennsylvania (Philadelphia, PA)
    …for IITs where collaborating physician is the Principal Investigator. Assist in analyzing clinical data to determine response and clinical outcomes; ... research performed. He/she will be responsible for all aspects of clinical trial coordination including subject recruitment, detailed data entry, subject… more
    University of Pennsylvania (08/08/25)
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  • Clinical Study Build Programmer

    Lilly (Indianapolis, IN)
    … trial data collection databases, including the mapping, testing and normalization of data into a clinical data warehouse. This requires an in-depth ... Data and Analytics colleagues such as the Clinical Data Associate, Clinical ...management, database programming or system validation experience in the clinical , pharmaceutical, biotech, CRO or regulatory agency… more
    Lilly (07/30/25)
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  • Clinical Research Coordinator III

    HonorHealth (AZ)
    …May be responsible for the following: collecting, verifying, organizing, completes and records clinical information and data in case report forms, CRF tracking, ... reviewing validation, updating, SAE reconciliation, lab data reconciliation, query resolution and recording clinical information and data in case report… more
    HonorHealth (06/18/25)
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  • Senior Manager, Clinical Project Management

    Sumitomo Pharma (Pierre, SD)
    …and communication with cross-functional teams to ensure proper execution and conduct of the clinical trial; generates quality clinical data . + Serves as ... including budget and timelines. + Monitors the status of clinical data collection of assigned clinical...and deliver program/study updates. + Coordinates the delivery of clinical trial supplies in collaboration with CRO … more
    Sumitomo Pharma (09/03/25)
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  • Clinical Trial Manager

    GRAIL (Menlo Park, CA)
    …mitigations and implements mitigations with cross-functional team and manager support + Monitors clinical data entry progress and follows up on incomplete ... terms + Works cross functionally with other departments such as Legal, Clinical Data Management, Biospecimen Management, Finance, Clinical Compliance,… more
    GRAIL (08/27/25)
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  • Clinical Research Associate ll

    Abbott (Alameda, CA)
    …and audit Trial Master File to ensure inspection readiness. + Perform review of clinical data listings for completeness and accuracy, and escalate issues to the ... experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data… more
    Abbott (08/08/25)
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  • Principal Scientist, Veterinary Clinical…

    Merck (West Point, PA)
    …Not Indicated **Valid Driving License:** No **Hazardous Material(s):** n/a **Required Skills:** Clinical Data Interpretation, Clinical Judgment, Clinical ... organization, these interpretations will offer a thorough analysis of clinical pathology data , including correlations to toxicokinetic...clinical pathologist in biotech, pharma or at a CRO is a plus, but not required + Excellent… more
    Merck (06/10/25)
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  • Clinical Trials Manager

    Gilead Sciences, Inc. (Foster City, CA)
    …policies and regulatory guidelines to provide timely delivery of high quality clinical data to support global registration and commercialization of Gilead's ... Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans, Clinical Study Report + Coordinates data review to support interim/final … more
    Gilead Sciences, Inc. (08/13/25)
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  • Senior Clinical Research Director, I&I

    Sanofi Group (Bridgewater, NJ)
    …activities (eg pressure test and cluster feasibility, medical review and validation of clinical data , study risk assessment) + Contribute to the clinical ... data , medical information for the study team, medical advisors/ Clinical Project Leaders from Clinical Study Units,...+ At least 4 years in pharmaceutical industry or CRO , previous experience in clinical development **Why… more
    Sanofi Group (07/06/25)
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  • Principal Analyst, Clinical Programming…

    AbbVie (North Chicago, IL)
    …Analysis System (SAS) programs for creation of Analysis Data Model (ADaM) data sets following Clinical Data Interchange Standards Consortium (CDISC) ... 6 years: + performing in statistical programming in the CRO or Pharmaceutical Industry; + applying SAS programming concepts...in CNS. With either alternative, must have experience preparing clinical data for at least 1 FDA… more
    AbbVie (08/21/25)
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