• Associate Director

    Sumitomo Pharma (Raleigh, NC)
    …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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  • Associate Director

    United Therapeutics (Raleigh, NC)
    …or pharma regulatory experience with a Bachelor's Degree in life sciences, quality, regulatory affairs or a related area of study or 10+ years of biologic ... pharma regulatory experience with a Master's Degree in life sciences, quality, regulatory affairs or a related area of study or 7+ years of biologic or… more
    United Therapeutics (09/27/25)
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  • Medical Affairs Associate

    IQVIA (Durham, NC)
    …may require onsite visits to clients. **Role and responsibilities** + Represent Medical Affairs on the content review committee as the lead Medical Reviewer / ... line with client's strategy and expectations + Effectively collaborate with Commercial, Regulatory , and Legal business partners to provide strategic input and drive… more
    IQVIA (08/12/25)
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  • Dir-Government Affairs

    Lowe's (Mooresville, NC)
    **Your Impact** The primary purpose of the Director , Government Affairs position is to lead the advocacy on behalf of Lowe's in the company's key strategic and ... markets for the assigned markets - South Divisions and/or Headquarters State. This Director position leads the advocacy before state and local legislative and … more
    Lowe's (09/16/25)
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  • Associate Director , Data Sciences,…

    IQVIA (Durham, NC)
    ** Associate Director , Data Sciences, Safety, and Regulatory FSP Sales** Associate Director , Data Sciences, Safety, and Regulatory , FSP Sales will ... for the Data Management, Biostatistics, Programming, Medical Writing, Lifecycle Safety, and Regulatory Affairs functions - and will be responsible for achieving… more
    IQVIA (10/01/25)
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  • Associate Director , Small Molecule…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    ** 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. (08/27/25)
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  • Associate Director , QA Engineering…

    United Therapeutics (Research Triangle Park, NC)
    …individual expertise and mentoring or developing a member of your team. The Associate Director , QA Engineering will provide advanced support and subject matter ... across multiple functional groups (eg, Research and Development, Manufacturing, Validation, Regulatory Affairs , etc.). Negotiate and manage expectations across… more
    United Therapeutics (09/26/25)
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  • Associate Director , Statistics,…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …data scientists and data programmers, and external stakeholders including Medical Affairs , Value and Real World Evidence to provide end-to-end statistical expertise ... approve tables, listings and graphs specifications. + Closely work with Medical Affairs to support statistical design, conduct secondary analyses of clinical and… more
    Otsuka America Pharmaceutical Inc. (09/05/25)
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  • Field Director , Medical Science Liaison…

    Grifols Shared Services North America, Inc (Benson, NC)
    …for the therapeutic area(s). + Partners with the Medical Directors, National MSL Sr Director , and North America Medical Affairs Sr Director to develop ... and regions. The primary responsibility of the MSL Field Director is the management, performance, and coaching of a...of field medical plans, strategy, and activities within Medical Affairs , as aligned with goals and objectives. This position… more
    Grifols Shared Services North America, Inc (07/24/25)
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  • Senior Scientist Regulatory Compliance

    Cambrex High Point (High Point, NC)
    …submission of CAPA plans, Change Requests, and Deviations in coordination with the Associate Director , Quality Assurance + Author and Revise Quality Documents ... GXP/QA/ regulatory compliant pharmaceutical laboratory environment or Quality Assurance/ Regulatory Affairs role (prefer late phase/commercial experience).… more
    Cambrex High Point (07/17/25)
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