• Associate Director , Global

    Takeda Pharmaceuticals (Atlanta, GA)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Project Management and Strategic ... Regulatory Affairs Team. **How you will contribute:** + As Associate Director , Global Regulatory Project Management and Strategic Planning, you… more
    Takeda Pharmaceuticals (06/07/24)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Atlanta, GA)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Labeling Lead where you will be responsible ... You 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 (06/07/24)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Atlanta, GA)
    …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned products… more
    Takeda Pharmaceuticals (06/13/24)
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  • Associate Director - Pharmacometrics

    Merck (Atlanta, GA)
    …component of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... Associate Director will work with scientists within...analyses + Developing and maintaining a comprehensive understanding of global regulatory expectations for small molecules and… more
    Merck (05/02/24)
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  • Associate Director , Quantitative…

    Merck (Atlanta, GA)
    …Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global Clinical Development ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
    Merck (05/10/24)
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  • Regulatory Senior Associate

    ADM (Kennesaw, GA)
    …the products in the North American Market. The Senior Manager works in conjunction with the Global Director or Regulatory Compliance H&W and the Director ... **83651BR** **Job Title:** Regulatory Senior Associate **Department/Function:** Legal, Compliance,...the products in the market **Job Responsibilities:** + Leverage global regulatory compliance of the H&W portfolio… more
    ADM (05/15/24)
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  • Associate Director , Combination…

    Merck (Atlanta, GA)
    …Medical Device and Combination Product (MDCP) Quality Assurance Operations team, the Associate Director Quality Engineering & Quality Assurance is responsible ... reviewing and approving medical device/combination product documentation to support regulatory filings and audits of data, policies, procedures, and systems… more
    Merck (05/31/24)
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  • Associate Director , IMO

    Ford Motor Company (Atlanta, GA)
    …ready to change the way the world moves? **In this position ** As the Associate Director of M&A Integration, you will lead the strategic integration of merged ... smooth transition. + Ensure that all integration activities comply with regulatory requirements and company policies. + Drive synergy identification and realization,… more
    Ford Motor Company (06/13/24)
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  • Program Associate Director

    Zimmer Biomet (Atlanta, GA)
    …included, respected, empowered, and recognized. **What You Can Expect** The Program Associate Director will oversee lifecycle management business processes to ... of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a...- Research, Business Development, Finance, Clinical, Commercial, Legal and Regulatory . + Analyze the data related to the portfolio… more
    Zimmer Biomet (05/30/24)
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  • Associate Clinical Lead Director

    IQVIA (Atlanta, GA)
    …In depth knowledge of, and skill in applying applicable clinical research regulatory requirements; ie, Good Clinical Practice (GCP) and International Conference on ... travel _This is a remote / WFH opportunity_ IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the… more
    IQVIA (06/07/24)
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