• Clinical Medical Editor

    Actalent (Chicago Heights, IL)
    …Skills + Proven source verification and proofreading abilities. + Experience with PromoMats, Clinical Research , Regulatory Affairs , and Clinical ... submissions. + Research promotional claims and perform data mining using Clinical Study Reports (CSRs) and resources from the company library. + Organize and… more
    Actalent (10/18/25)
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  • Quality Assurance & Compliance Intern (Graduate)

    AbbVie (North Chicago, IL)
    …life sciences (eg, biology, biochemistry), bioengineering, biomedical engineering, public health, clinical research , regulatory affairs , biomedical ... AbbVie Quality System in R&D. The team ensures that clinical research and operations consistently meet regulatory requirements, internal standards, and… more
    AbbVie (10/10/25)
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  • Director, Pipeline and External Innovation…

    AbbVie (North Chicago, IL)
    …government affairs , investor relations, legal, finance, discovery research , clinical development, regulatory affairs , medical affairs , and ... execution for scientific data disclosures (eg, congress presentations, publications), clinical development milestones, regulatory filings, and pre-commercial… more
    AbbVie (09/04/25)
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  • Senior Regulatory Specialist, Data…

    Cardinal Health (Springfield, IL)
    …as well as clinical research and manufacturing process consulting. Regulatory Affairs plans, coordinates and implement regulatory strategies for ... **_What Regulatory Affairs contributes to Cardinal Health_**...the integrity of regulatory data used for regulatory submissions, clinical evaluations and post-market surveillance.… more
    Cardinal Health (10/10/25)
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  • Vice President, Regulatory Affairs…

    Sumitomo Pharma (Springfield, IL)
    …+ Provide strategic and operational leadership to the Marketing Brand Teams, Legal, Medical Affairs and Clinical Research in the development of advertising ... and experienced leader for the position of **Vice President, Regulatory Affairs Oncology** . The candidate must...individual will be responsible for leading development of all non- clinical and clinical regulatory strategies… more
    Sumitomo Pharma (09/23/25)
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  • Associate Director, Regulatory…

    Sumitomo Pharma (Springfield, IL)
    …highly motivated, and experienced individual for the position of **Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part of the ... Global Regulatory Affairs (GRA) team based in the...terminology, and FDA and ICH regulations/guidance documents specific to clinical research and general product development in… more
    Sumitomo Pharma (10/11/25)
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  • Director, Regulatory Affairs

    Sumitomo Pharma (Springfield, IL)
    …seeking a dynamic, highly motivated, and experienced individual for the position of **Director Regulatory Affairs ** . The Director is part of the Global ... Regulatory Affairs (GRA) team based in the...Regulatory Affairs (GRA) team based in the US. He/she will...medical terminology, and FDA and ICH regulations/guidances specific to clinical research and general product development in… more
    Sumitomo Pharma (09/09/25)
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  • VP, Regulatory Affairs R&D Biopharma

    Sumitomo Pharma (Springfield, IL)
    …highly motivated, and experienced individual for the position of Vice President, Regulatory Affairs , Biopharma R&D. This position leads the Regulatory ... CNS assets. **Job Duties and Responsibilities** **_Regulatory Strategy_** + Develop and Manage Regulatory Affairs Strategy + Develop and gain approval for … more
    Sumitomo Pharma (09/10/25)
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  • Senior Principal Regulatory Affairs…

    Bausch + Lomb (Springfield, IL)
    …Bachelor degree or equivalent, Master degree preferred + Minimum of 8 years in Regulatory Affairs or relevant experience in a regulated environment + Ability to ... + Strong business acumen and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative ideas to promote a successful… more
    Bausch + Lomb (09/06/25)
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  • Regulatory Affairs Lead, Oncology…

    Astellas Pharma (Northbrook, IL)
    …& People Management** + Supports an environment to enable each member of the Regulatory Affairs team to optimally operate in the matrix environment of GRA, ... discipline associated with pharmaceutical development or product oversight; 3 years in regulatory affairs preferred. + Strong scientific knowledge and … more
    Astellas Pharma (09/19/25)
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