• Medical Director, Clinical Development

    AbbVie (North Chicago, IL)
    …understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. ... of clinical trials or research activities of one or more clinical development programs. Participates in cross-functional teams to generate, deliver, and interpret… more
    AbbVie (08/13/25)
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  • Associate Director, Quantitative Pharmacology,…

    Otsuka America Pharmaceutical Inc. (Springfield, IL)
    …and reporting of **pharmacometrics** studies, while providing input into all phases of drug development including, but not limited to dose finding, dose ... member on other key projects as needed and **supports model-based drug development strategies** for ongoing projects. **Qualifications/ Required** Knowledge,… more
    Otsuka America Pharmaceutical Inc. (08/16/25)
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  • Associate Medical Director, Clinical…

    AbbVie (North Chicago, IL)
    …understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. May ... interpretation of clinical trials or research activities of a clinical development program. Participates in cross-functional teams to generate, deliver, and… more
    AbbVie (08/13/25)
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  • Associate Scientific Director, Clinical…

    AbbVie (North Chicago, IL)
    …understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. May ... interpretation of clinical trials or research activities of a clinical development program. Participates in cross-functional teams to generate, deliver and interpret… more
    AbbVie (08/08/25)
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  • Account Executive, Late Phase

    Catalent Pharma Solutions (Arlington Heights, IL)
    …holidays **Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 ... Team, and your primary role is to evaluate and assess contract development and manufacturing opportunities with Rx pharmaceutical customers. The Business … more
    Catalent Pharma Solutions (07/22/25)
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  • Sr Dir Pharmacy Trade Relations - Remote

    Prime Therapeutics (Springfield, IL)
    …years of related work experience in healthcare, pharmacy benefit management (PBM), pharmaceutical sales, analytical contracting or business development ; also to ... Pharmacy Trade Relations - Remote **Job Description** The Sr Director, Pharmaceutical Trade Relations is responsible for managing Prime's Trade Relations program(s)… more
    Prime Therapeutics (08/08/25)
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  • Manager, Quality Risk Management

    AbbVie (North Chicago, IL)
    …Risk Management (QRM) activities for AbbVie products such as Combination, Pharmaceutical and medical devices. Support the strategic direction to ensure business ... requirements. Assure proper integration for AbbVie products such as device, combination, drug and biologics regulations. + Areas of direct responsibility include … more
    AbbVie (07/10/25)
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  • Senior Manager, Global Regulatory Affairs

    Otsuka America Pharmaceutical Inc. (Springfield, IL)
    …written communication skills. - Solid working knowledge and understanding of the drug development process, laws, regulations, and guidelines including FDA, ICH, ... Center at: https://www.ic3.gov , or your local authorities. Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization,… more
    Otsuka America Pharmaceutical Inc. (06/19/25)
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  • Associate Director, Medical Affairs Omnichannel

    Otsuka America Pharmaceutical Inc. (Springfield, IL)
    …Center at: https://www.ic3.gov , or your local authorities. Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, ... with deep experience in the ever-developing Omnichannel effort in the pharmaceutical industry with a focus on Medical Affairs initiatives. **Key Responsibilities:**… more
    Otsuka America Pharmaceutical Inc. (07/15/25)
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  • Associate Director, NPI Product Quality

    AbbVie (North Chicago, IL)
    …agency regulations worldwide. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), Intermediates, and Drug Products produced ... by developing and/or reviewing of chemistry, manufacturing and controls documents and Drug Master files/Certificate if suitability of monographs of the Ph. Eur.… more
    AbbVie (07/09/25)
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