• Associate Director , Global…

    Takeda Pharmaceuticals (Indianapolis, IN)
    Regulatory Affairs Team. **How you will contribute:** + As Associate Director , Global Regulatory Project Management and Strategic Planning, you ... life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Project...through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global … more
    Takeda Pharmaceuticals (05/09/24)
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  • Associate Director , GMP Quality…

    Sumitomo Pharma (Indianapolis, IN)
    ** Associate Director , GMP Quality Control** Sumitomo Pharma America (SMPA) is focused on delivering therapeutic and scientific breakthroughs in areas of critical ... seeking a dynamic, highly motivated, and experienced individual for the position of Associate Director of GMP Quality Control, who oversees GMP compliance of… more
    Sumitomo Pharma (04/19/24)
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  • Associate Director , Global Labeling

    Takeda Pharmaceuticals (Indianapolis, IN)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Labeling Lead where you will be responsible for the ... will serve as the regulatory expert for labeling on the Global Regulatory Affairs subteam to ensure that regulatory labeling requirements are met for… more
    Takeda Pharmaceuticals (03/29/24)
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  • Regional Associate Director

    Bristol Myers Squibb (Indianapolis, IN)
    …work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director , Clinical Nurse Consultant** _The Clinical Nurse Consultant ... (CNC) Associate Director is the leader of a...in other regional/field-based positions from the commercial and medical affairs organizations + Promote open dialogue with cross functional… more
    Bristol Myers Squibb (04/20/24)
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  • Associate Director - Device Safety…

    Lilly (Indianapolis, IN)
    …and volunteerism. **Purpose:** The purpose of the Medical Device Safety Scientist Associate Director role is to leverage clinical and scientific expertise ... areas relevant to drug discovery or development, eg epidemiology, toxicology, pharmacovigilance, regulatory affairs + Experience within Global Patient Safety or… more
    Lilly (04/17/24)
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  • Center Medical Director (CMD)

    CSL Plasma (Indianapolis, IN)
    …Staff Associates for completion of training and recommendation for certification by Regulatory Affairs . Functionally directs the Center Medical Staff. Provides ... Usually serves as the primary center physician registered as the Laboratory Director with the Food and Drug Administration (FDA). **Job Description** + Serves… more
    CSL Plasma (04/16/24)
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  • Contract Center Medical Director /Center…

    CSL Plasma (Hobart, IN)
    …Staff Associates for completion of training and recommendation for certification by Regulatory Affairs . Functionally directs the Center Medical Staff. Provides ... as or delegates to another appropriate physician the duties of "laboratory director ", "technical consultant", or "clinical consultant" as prescribed by the Clinical… more
    CSL Plasma (04/16/24)
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  • Associate Vice President-Clinical Design…

    Lilly (Indianapolis, IN)
    …additional items including but not limited to protocols, publications, regulatory interactions, internal executive and governance presentations, external key opinion ... Understand how design elements influence the ability to deliver on new regulatory expectations (eg decentralization of clinical trials, increase racial and ethnic… more
    Lilly (02/29/24)
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  • Associate Vice President - Clinical Design…

    Lilly (Indianapolis, IN)
    …additional items including but not limited to protocols, publications, regulatory interactions, internal executive and governance presentations, external key opinion ... Understand how design elements influence the ability to deliver on new regulatory expectations (eg decentralization of clinical trials, increase racial and ethnic… more
    Lilly (05/10/24)
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