• Associate Director , Global

    Takeda Pharmaceuticals (San Juan, PR)
    …activities pertaining to global and local labeling compliance and quality within Global Regulatory Affairs . + Partners with internal stakeholders and ... to the best of my knowledge. **Job Description** The Regulatory Affairs -Labeling, Associate Director is...external CRO partners such as Global Regulatory Compliance, Global Labeling,… more
    Takeda Pharmaceuticals (11/27/24)
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  • Director Global Regulatory

    Takeda Pharmaceuticals (San Juan, PR)
    …understands probabilities of technical success for the solutions. + Effectively represent the Global Regulatory Affairs (GRA) function in senior level ... for providing strategic guidance and oversight for the delivery of global regulatory strategies to support development of biomarkers, diagnostic tests, devices… more
    Takeda Pharmaceuticals (12/06/24)
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  • Associate Director , Global

    Takeda Pharmaceuticals (San Juan, PR)
    Regulatory Project Management and Strategic Planning - GI2 TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the ... implementing process changes through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global more
    Takeda Pharmaceuticals (10/24/24)
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  • Associate Director , Global Labeling…

    Takeda Pharmaceuticals (San Juan, PR)
    …+ Appropriately escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned ... life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will...+ Working within Labeling Team and GRA + Represents Global Labeling at Global Regulatory more
    Takeda Pharmaceuticals (10/16/24)
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  • Associate Director , Global Patient…

    Takeda Pharmaceuticals (San Juan, PR)
    …Liaise with and advise study teams including Clinical Science, Data Management, Regulatory Affairs , and other functional areas locally/globally on matters ... of clinical trial and Pharmacovigilance methodologies including detailed comprehension of global regulatory requirements. + Good cross-cultural understanding and… more
    Takeda Pharmaceuticals (12/06/24)
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  • Senior Manager, Biostatistics

    Edwards Lifesciences (San Juan, PR)
    …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more
    Edwards Lifesciences (10/28/24)
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