• Clinical Trial Associate

    Astellas Pharma (Northbrook, IL)
    …in remote work are encouraged to apply. **Purpose and Scope:** This position will assist the Clinical Trial Lead (s) and Clinical Trial Manager(s) in the ... regulatory commitment trials (interventional and non-interventional). This position is accountable to the clinical trial team for the support of the trial more
    Astellas Pharma (10/22/24)
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  • Scientific Director, Clinical Scientist,…

    AbbVie (South San Francisco, CA)
    …+ Strong track record of collaboration in a cross-functional setting. + Clinical trial experience in the pharmaceutical industry, academia, or equivalent ... for late-stage assets. + May oversee the work of Associate Scientific Directors and/or of Clinical Scientists...is preferred. + Knowledge of clinical trial methodology, regulatory and compliance requirements… more
    AbbVie (09/25/24)
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  • Associate Director - Clinical

    Lilly (Indianapolis, IN)
    …for people who are determined to make life better for people around the world. Clinical Trial Foundations as part of Clinical Design, Delivery & Analytics ... (CDDA) provides leadership in the strategy and development of contemporary clinical trial processes, technologies, information, and capabilities and in shaping… more
    Lilly (09/24/24)
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  • Associate Clinical Site Lead

    Abbott (Philadelphia, PA)
    …product and disease state knowledge, procedure support (as needed), procedure outcomes and early indication of trends, clinical trial enrollment, and ICH-GCP ... working mothers, female executives, and scientists. **The Opportunity** The ** Associate Clinical Site Lead** for the Philadelphia,...needed, provide clinical and technical expertise for clinical trial procedure support + Attend study… more
    Abbott (10/18/24)
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  • Senior Associate - Clinical Study…

    Lilly (IN)
    Clinical Study Build Programmer is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and ... collection systems and associated data repository mappings for a trial or set of trials within a program using...Partner with Data and Analytics colleagues such as the Clinical Data Associate , Clinical Data… more
    Lilly (10/27/24)
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  • Associate Director, Precision Medicine…

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    …This will be done in collaboration with Precision Medicine Strategy Leads, Clinical Trial Management, Clinical Laboratory Operations Management, Global ... The Associate Director, Precision Medicine Clinical Laboratory...laboratory management + Demonstrate relevant knowledge and understanding of clinical laboratory trial requirements on the program… more
    Regeneron Pharmaceuticals (10/23/24)
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  • Associate Director, Clinical

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    …development projects through early and/or late phase development. The Associate Director reports to the Director, Clinical Sciences and collaborates ... We are seeking an Associate Director to join out Oncology Clinical...clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments + Authors… more
    Regeneron Pharmaceuticals (10/10/24)
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  • Senior Associate - Clinical Supply…

    Lilly (Indianapolis, IN)
    …Commercial Product, and Ancillary strategies to ensure technology enables clinical trial design and execution. The Associate , Clinical Supply Systems, ... oversight, and management of clinical processes, information, and technologies within Clinical Trial Foundations (CTF) organization, Clinical Supply and… more
    Lilly (10/16/24)
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  • Associate Director, Clinical

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments. Authors and/or reviews documents ... The Associate Director, Clinical Sciences contributes to...Utilizes proficient scientific expertise to propose, design, and execute clinical research and development studies for early more
    Regeneron Pharmaceuticals (10/16/24)
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  • Associate Medical Director Neuroscience…

    AbbVie (Irvine, CA)
    …supervision. + Strong desire to collaborate in a cross-functional setting. + Clinical trial experience in the pharmaceutical industry, academia, or equivalent ... is preferred. + Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of… more
    AbbVie (10/16/24)
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  • Clinical Research Clinician,…

    Pfizer (New Haven, CT)
    …and Pfizer SOPs, Work instructions and Guidances. + Develops a good working knowledge of clinical trial activities within the industry and passes this on to less ... Clinical Research Unit (PCRU) and has responsibilities and accountabilities for trial oversight involving all clinical and medical aspects of study conduct.… more
    Pfizer (10/12/24)
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  • Associate Medical Director, Clinical

    Takeda Pharmaceuticals (Cambridge, MA)
    …​The Associate Medical Director leads and drives strategy for clinical studies focused on neurodegenerative disorders within the overall global clinical ... and empower you to shine? Join us as an Associate Medical Director Neurodegenerative Disorders in our Neuroscience Therapeutic...with the global strategy. + May act as Global Clinical Lead for an early or a… more
    Takeda Pharmaceuticals (09/25/24)
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  • Medical Director, Oncology Early

    AbbVie (South San Francisco, CA)
    …Completion of a subspecialty fellowship is desirable. + At least 3 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent. + ... other program documents. + May oversee the work of Associate Medical and/or Scientific Directors, and of Clinical...in ADC and/or CART development preferred + Knowledge of clinical trial methodology, regulatory and compliance requirements… more
    AbbVie (09/20/24)
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  • Clinical Research Associate

    Touro University (Hawthorne, NY)
    Overview Responsible for pre- clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen ... to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and...children + Legal plan + Employee Assistance Program + Early -Release Fridays (October - March) + Generous Paid Time… more
    Touro University (10/25/24)
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  • Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    …screen patients for Oncology clinical research trials; collect and submit clinical trial patient data. Perform various administrative duties, which may ... Job Summary: The Clinical Research Associate I will coordinate...sites, primarily involving investigational medications and radiation therapy, including early or late phase FDA-regulated trials. Ensure compliance with… more
    SUNY Upstate Medical University (10/16/24)
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  • Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    …screen patients for Oncology clinical research trials; collect and submit clinical trial patient data. Perform various administrative duties, which may ... Job Summary: The Clinical Research Associate I will coordinate...satellite sites, primarily involving investigational medications and treatments, including early or late phase FDA-regulated trials. Ensure compliance with… more
    SUNY Upstate Medical University (09/28/24)
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  • Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    …and screen patients for clinical research trials; collect and submit clinical trial patient data. Perform various administrative duties, which may include ... Coordinate multiple research trials for the Institute for Global Health, including early to late phase FDA-regulated trials, and ensure compliance with federal… more
    SUNY Upstate Medical University (10/16/24)
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  • Clinical Research Associate II

    SUNY Upstate Medical University (Syracuse, NY)
    …and screen patients for clinical research trials; collect and submit clinical trial patient data. Perform various administrative duties, which may include ... Coordinate various research trials for the Institute for Global Health, including early or late phase FDA-regulated trials, and ensure compliance with federal… more
    SUNY Upstate Medical University (10/16/24)
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  • Clinical Research Coordinator POEMS Team

    University of Colorado (Aurora, CO)
    …protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial + Perform informed consent process or ensures that ... phone contacts and personal interviews + Schedule subject participation in research clinical trial , coordinating availability of necessary space, and clinical more
    University of Colorado (09/08/24)
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  • Research Services Senior Principal Professional…

    University of Colorado (Aurora, CO)
    …protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial + Perform informed consent process or ensures that ... and personal interviews + Schedule subject participation in research clinical trial , coordinating availability of necessary space,...Bachelor of Science in Nursing (BSN) degree + An Associate Degree in Nursing (ADN) degree and two (2)… more
    University of Colorado (09/08/24)
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