• Canfield Scientific, Inc (Parsippany, NJ)
    …analysis services for the pharmaceutical, biotechnology and cosmetics industries supporting global clinical trials providing primary endpoint data and ... We are seeking a motivated and detail-oriented Qualitative Clinical Outcomes Researcher , with strong medical writing skills to join our fast-paced, collective team… more
    job goal (12/07/25)
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  • Rovia Clinical Research (Miami, FL)
    …participants on time. Responsibilities: Serve as Principal Investigator across high-quality clinical trials in major therapeutic indications (including diabetes, ... with best-in class retention, rapid study-start up and high-quality data . The network is a preferred partner to leading...of experience as a PI or Sub-Investigator in FDA-regulated clinical trials . Strong clinical judgment… more
    job goal (12/08/25)
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  • Clinical Trials - Clinical

    Lilly (Indianapolis, IN)
    …position 3 days onsite/2 days remote **Purpose:** This role is responsible for trial level clinical data strategy including database structure, content ... with key study partners to define, implement, and deliver clinical data management packages. This role is... trial leadership and ownership for a particular trial , set of trials , or programs. **Primary… more
    Lilly (09/25/25)
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  • Associate Manager, Clinical Trial

    Abbott (Austin, TX)
    …hospital payment codes and other claims data . + Basic understanding of clinical trial categorizations not limited to IDE studies, PM and categorization of ... 500,000 people with diabetes from routine fingersticks. The **Associate Manager of Clinical Trial Reimbursement** is responsible for implementing and managing … more
    Abbott (10/25/25)
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  • Research Scientist - Clinical

    Lilly (Indianapolis, IN)
    …channel strategy, and preparation of final reports and publications. + Participate in reporting of clinical trial data in Clinical Trial Registry ... of responsibility, the development, conduct and reporting of local clinical trials ; the implementation of global ...I and II studies where applicable), as well as non- clinical trial solutions/activities that are conducted in… more
    Lilly (12/05/25)
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  • Sr. Director - Clinical Development

    Lilly (Indianapolis, IN)
    …of external health care professionals according to guidelines above. + Participate in reporting of clinical trial data in Clinical Trial Registry ... gastroenterology therapeutic area will support early and late phase clinical trials for assets in the gastroenterology...clinical data relevant to the molecule. Clinical Research/ Trial / Execution and Support + Plans,… more
    Lilly (12/06/25)
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  • Clinical Trial Operations Intern

    AbbVie (North Chicago, IL)
    …in the Clinical Trial Operations (CTO) Internship Program at AbbVie. Clinical Trials are required before a new compound can be available for use ... clinical data collection, management, integration, and utilization within AbbVie clinical trials . This includes the operations and technology to enable … more
    AbbVie (10/04/25)
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  • Clinical Research Data Associate III…

    Cedars-Sinai (Los Angeles, CA)
    data for assigned research studies. This will include, designing forms for data collection, clinical data abstraction, processing data , maintaining ... producing project reports for studies. In addition, may supervise clinical research staff or clinical data...Work with bioinformatics in the development and maintenance of clinical trials management systems including validation of… more
    Cedars-Sinai (10/09/25)
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  • Clinical Business Analyst

    Insight Global (Boston, MA)
    …the IT organization. The BA will assist with enabling technologies that support Clinical Operations, Clinical Data Management, and Risk Based Monitoring ... CTMS, so they will need to have experience with clinical trial capabilities and comfortable working with...pharmaceutical industry * Clinical experience working with Clinical Operations, Clinical Data Management,… more
    Insight Global (09/27/25)
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  • Sr. Principal - Clinical Study Build…

    Lilly (Indianapolis, IN)
    … Study Build Programmer is responsible for leading and programming and testing clinical trial data collection databases, including the mapping, testing ... and associated data repository mappings for a trial or set of trials within a...a deep understanding of the technology used to collect clinical trial data + Effectively… more
    Lilly (11/03/25)
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