• Associate Director , US Advertising…

    Takeda Pharmaceuticals (Exton, PA)
    …to the best of my knowledge. **Job Description** ** Associate Director , US Advertising & Promotion Regulatory Review** **Takeda Pharmaceutical** **Lexington, ... the role:** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory Review...proposed promotional and disease state materials. + Collaborate with Regulatory Affairs , Medical, Legal, Commercial, and Compliance,… more
    Takeda Pharmaceuticals (02/13/25)
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  • Associate Director , Corporate…

    CSL Behring (King Of Prussia, PA)
    The Associate Director , Corporate Accounts (ADCA) is responsible for optimizing access, reimbursement, and profitability for CSL Behring's portfolio of brands in ... role in CSL Behring's commercial organization and reports to the Senior Director of Corporate Accounts. The ADCA is responsible for executing CSL Behring's… more
    CSL Behring (01/09/25)
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  • Associate Director , HCP Marketing

    Endo International (Malvern, PA)
    …looking for talented individuals to join our team. **Job Description Summary** The Associate Director , HCP Marketing (AD) will collaborate with the Orthopedic ... platform + Understand and adhere to FDA, DEA and internal regulatory affairs guidelines. + Develop advocacy strategy and resulting tactics while meeting… more
    Endo International (02/11/25)
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  • Associate General Counsel, Transactions

    Teva Pharmaceuticals (West Chester, PA)
    …people to make a difference with. **The opportunity** The Sr. Director , Associate General Counsel, Transactions & Corporate Affairs role reports directly to ... Associate General Counsel, Transactions Date: Feb 19, 2025...functions, including R&D, intellectual property, supply chain, finance, and regulatory affairs . This role will also help… more
    Teva Pharmaceuticals (02/20/25)
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  • Distinguished Scientist, Product Development Team…

    Merck (North Wales, PA)
    …a cross-functional Senior/ Executive Director group of experts in commercialization, regulatory affairs , statistics, medical affairs and manufacturing to ... teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We… more
    Merck (02/22/25)
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