• Associate Director, Operational Readiness,…

    Lilly (Indianapolis, IN)
    …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... is expansive, stretching across all functional areas of the site , requiring the Associate Director Operational Readiness to build breadth of knowledge and… more
    Lilly (09/22/25)
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  • Research Associate II - Noble/Jiang Labs…

    Cedars-Sinai (Los Angeles, CA)
    …the role of host defense in lung inflammation and fibrosis. The Research Associate II will perform routine and increasingly complex laboratory tasks and procedures ... maintenance. This position does not have supervisory responsibilities. The associate investigates molecular mechanisms of lung fibrosis, and participates in… more
    Cedars-Sinai (10/25/25)
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  • Quality Assurance Document Control…

    Catalent Pharma Solutions (Philadelphia, PA)
    …and approve batch records before production to ensure compliance with cGMP, clinical trial protocols, and blinding requirements. + Monitor production schedules ... Excellence for Clinical Supply Packaging, offering GMP secondary packaging and clinical labeling services. The site provides manual to fully automated… more
    Catalent Pharma Solutions (11/05/25)
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  • Associate Innovation Product Manager…

    BD (Becton, Dickinson and Company) (Tempe, AZ)
    …and promotion of prescription drugs preferred. + Familiarity with medical terminology and clinical trial methodologies preferred. + Ability to travel up to 20%, ... self. Become a **maker of possible** with us. As Associate Product Manager, Upstream, PI Vascular, you will be...of assigned products and spaces in conjunction with R&D, Clinical , Downstream Marketing, and other functions. You will be… more
    BD (Becton, Dickinson and Company) (10/31/25)
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  • Associate Director - Analytical Quality…

    Lilly (Indianapolis, IN)
    …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director - Analytical Quality Assurance ensures that laboratory...partners are carried out in accordance with global and site quality standards and/or are following current Good Manufacturing… more
    Lilly (10/22/25)
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  • GLOBAL Project Manager (FSP), Remote (US)

    ThermoFisher Scientific (Wilmington, NC)
    … study management/oversight, including significant study management support experience (eg clinical trial assistant/ associate or lead CRA). Experience ... the inspections.** ** Site relationship management** **Review and provide oversight of trial audits** **Proper and timely follow up to audit findings and CAPAs**… more
    ThermoFisher Scientific (11/06/25)
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  • Research Associate at the CTSA

    University of Pennsylvania (Philadelphia, PA)
    …(3) years). Applicants must have a Ph.D. degree. Responsibilities may include management of on- site activities for a new trial based out of the Connecticut Army ... of Medicine at the University of Pennsylvania seeks candidates for a Research Associate position in the Academic Support Staff. This appointment will be initially… more
    University of Pennsylvania (09/01/25)
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  • Strategy Consulting Associate (Summer 2026…

    IQVIA (New York, NY)
    …about optimizing a treatment's potential, covering various aspects ranging from trial design to reimbursement submissions to life cycle management. We advise ... to client audiences via teleconference or in face-to-face meetings at the client site + Cultivate professional relationships with members of the client team +… more
    IQVIA (11/05/25)
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  • Tenure-Track Physician, Scientist…

    University of Maryland, Baltimore (Baltimore, MD)
    …who are already exploring how data science can be merged with clinical trial methodologies in the context of a multi- site health system to facilitate ... scientist or physician-scientist with expertise in real world data and novel clinical trial design/execution with particular emphasis on oncology sciences to… more
    University of Maryland, Baltimore (10/13/25)
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  • NCTN Program Coordinator

    University of Colorado (Aurora, CO)
    …to CTEP and ensuring that the pharmacy worksheet accurately reflects pharmacy staff at each site . + Manage Clinical Trial Support Unit (CTSU) database and ... of the LAPS Executive Committee including compiling protocol and site -specific information on new study activations to be reviewed,...delinquent data (>90 day past due). + Submit monthly clinical trial pipeline reports for the project… more
    University of Colorado (11/14/25)
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