• Associate Director

    Sumitomo Pharma (Oklahoma City, OK)
    …currently seeking a dynamic, 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 US. He/She will primarily function as a regional regulatory leader… more
    Sumitomo Pharma (10/11/25)
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  • Regulatory Affairs Associate

    GRAIL (Oklahoma City, OK)
    …products with the FDA and/or global health authorities. + Support the US Regulatory Affairs team in preparing submissions such as PMAs, 510(k)s, post-approval ... and review of Standard Operating Procedures and policy guidelines within the regulatory affairs department. + Perform other duties as assigned. **Preferred… more
    GRAIL (12/03/25)
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  • Associate Director

    Otsuka America Pharmaceutical Inc. (Oklahoma City, OK)
    The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to ... + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory intelligence needs and strengthen and… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Associate Director , Congress…

    Otsuka America Pharmaceutical Inc. (Oklahoma City, OK)
    The Associate Director , Congress and Medical Education Strategy & Execution is responsible for executing and contributing to the global medical strategy and ... patient outcomes through deep scientific understanding and collaborative partnerships. The Associate Director partners closely with global and regional… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Associate Director , Biostatistics

    Otsuka America Pharmaceutical Inc. (Oklahoma City, OK)
    …needs and nutraceutical products for the maintenance of everyday health. As an Associate Director , Biostatistician, you will be a champion of Otsuka's culture ... statistical sections. + Discusses strategies with Global Clinical Development and Regulatory Affairs regarding study design and complex analysis issues,… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Associate Director , Small Molecule…

    Otsuka America Pharmaceutical Inc. (Oklahoma City, OK)
    ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to… more
    Otsuka America Pharmaceutical Inc. (11/25/25)
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  • Associate Director , Clinical…

    Lilly (Oklahoma City, OK)
    …partner closely with internal Lilly teams (including Clinical Development and Medical Affairs ) to ensure that insights from the field shape development strategies ... clarity. Where applicable the CRL may also represent Investigator Engagement with Regulatory and External Bodies and help shape the country-level clinical trial… more
    Lilly (12/02/25)
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  • Associate Director , Medical…

    Otsuka America Pharmaceutical Inc. (Oklahoma City, OK)
    …to address strategic objectives to business partners. + Work closely with medical affairs , marketing, and IT teams to ensure alignment and integration of omnichannel ... Research, Analytics, Otsuka Information Technology (OIT), Sales Operations, and Medical/ Regulatory /Legal integrated business partners. **Minimum Qualification:** + Bachelor's degree… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Manager, Medical Core Content - Rare Disease

    Otsuka America Pharmaceutical Inc. (Oklahoma City, OK)
    …internal and external regulations. This position reports directly to the Associate Director , CNS Scientific Communications. **Job Description** **Key ... Include:** **Core Content Development** + Under the guidance of the Associate Director , Medical Communications, draft and maintain high-priority, foundational… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Trial Master File (TMF) Specialist Oncology

    Sumitomo Pharma (Oklahoma City, OK)
    …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director , Clinical Business Operations, the specialist ensures accountable ... system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements. + Act as… more
    Sumitomo Pharma (11/05/25)
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