• Research Associate II - Community Outreach…

    Houston Methodist (Houston, TX)
    …in publication and grant writing at PI/Faculty direction. + Determines specific research project goals and objectives to be attained. Assumes responsibility ... including narrative development and supporting documents** Knowledge of community engaged research approaches and cancer prevention and control topics** Ability to… more
    Houston Methodist (10/31/25)
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  • Senior Research Technologist - Gaudette Lab

    Cleveland Clinic (Cleveland, OH)
    …welfare standards. Responsibilities include animal colony maintenance, laboratory organization, regulatory compliance and supporting general research activities, ... daily project protocols. + Collect, prepare, and maintain required research documentation, including informed consent records, case records, clinical notes,… more
    Cleveland Clinic (10/18/25)
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  • Associate Director, Neuroimmunolgy Clinical

    Bristol Myers Squibb (Princeton, NJ)
    …the Global Research organization in BMS and leads late stage clinical , pharmacological and translational research and development activities for the pipeline ... and supports late stage portfolio for regulatory , translational development and life cycle management. Translational Development drives strategy across core… more
    Bristol Myers Squibb (10/28/25)
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  • Director, Quantitative Clinical

    Takeda Pharmaceuticals (Cambridge, MA)
    …highly innovative treatments to patients. These scientists (from quantitative clinical pharmacology, statistics, programming, outcomes research and epidemiology, ... simulation approaches (eg, QSP, MBMA) to inform internal decisions and external regulatory interactions. + Represents Clinical Pharmacology in meetings with… more
    Takeda Pharmaceuticals (09/25/25)
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  • Group Medical Director, Clinical

    AbbVie (North Chicago, IL)
    …responsibilities may include supervision of matrix team members and serving as the Clinical Research representative to lend clinical development and medical ... the pharmaceutical industry, academia, or equivalent. + Ability to run a complex clinical research program independently. + Proven leadership skills and ability… more
    AbbVie (11/07/25)
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  • Senior Scientific Director, Clinical

    AbbVie (Irvine, CA)
    …Co- Chair, responsibilities may include supervision of matrix team members; serving as Clinical Research representative to lend clinical development or ... cross-functional and translational development preferred. *Ability to run a complex clinical research program independently. *Proven leadership skills and… more
    AbbVie (11/07/25)
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  • Medical Director, Clinical Development…

    AbbVie (North Chicago, IL)
    …Chair, responsibilities may include supervision of matrix team members and serving as Clinical Research representative to lend clinical development and ... the pharmaceutical industry, academia, or equivalent. + Ability to run a complex clinical research program independently. + Proven leadership skills and ability… more
    AbbVie (08/13/25)
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  • Research Associate III

    Alaka'ina Foundation Family of Companies (San Antonio, TX)
    …IACUC/IRB requirements. + Ability to develop and coordinate the implementation of clinical research studies, including regulatory requirements, maintenance ... Research Associate III Location TX - San Antonio...personnel. + Assists PI in tracking and updating established project budgets. + Assist the Government Support Agreements Manager… more
    Alaka'ina Foundation Family of Companies (09/24/25)
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  • Associate Director, Clinical Operations…

    CSL Behring (King Of Prussia, PA)
    …area preferred. Other degrees and certifications considered if commensurate with related clinical research experience (eg, diploma or associate degree RN, ... medical technologist). + As a guide, a minimum of 10 years' relevant clinical research (or related) experience within the pharmaceutical industry. + Previous… more
    CSL Behring (11/06/25)
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  • Sr. Principal - Clinical Study Build…

    Lilly (Indianapolis, IN)
    …therapeutic/scientific knowledge in the field of research + Society of Clinical Data Management certification + Project management experience + Familiarity ... data management, database programming or system validation experience in the clinical , pharmaceutical, biotech, CRO or regulatory agency sectors) + Qualified… more
    Lilly (11/03/25)
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