• Associate Director , CMC Regulatory

    J&J Family of Companies (Spring House, PA)
    Associate Director , CMC Regulatory Affairs - 2406221330W **Description** Johnson & Johnson is recruiting for an Associate Director , CMC Regulatory ... and is in alignment with the strategies of global regulatory affairs , the therapeutic area, commercial, regional...senior member of the department. + Reviews CMC regulatory dossiers for global submissions throughout the product lifecycle… more
    J&J Family of Companies (11/07/24)
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  • Director , Global Regulatory

    Merck (Upper Gwynedd, PA)
    **Job Description** We are seeking a Director (Principal Scientist), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... advance our pipeline and drive our strategic priorities. The Director , Principal Scientist | Regulatory Affairs... agencies. + Reports to Associate Vice President, Executive Director , or Senior Director in… more
    Merck (10/31/24)
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  • Senior Principal Scientist ( Senior

    Merck (North Wales, PA)
    **Job Description** We are seeking a Senior Director ( Sr . Principal Scientist) Global Regulatory Affairs Liaison with a visionary, growth-oriented ... drive our strategic priorities. **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs...external to GRACS. **Key Functions** + Reports to Executive Director or Associate Vice President, General Medicine + Works… more
    Merck (10/31/24)
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  • Associate Director , Advertising…

    Merck (North Wales, PA)
    **Job Description** Reports to the Director / Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is ... and approval of all US promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional… more
    Merck (10/31/24)
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  • Sr . Manager, Strategic Projects

    CSL Behring (King Of Prussia, PA)
    …within Medical Affairs . Based on knowledge of worldwide legal and regulatory requirements and internal standards, you will oversee the revision of existing ... **The Opportunity** Reporting to the Executive Director , Strategic Projects, you will identify, oversee and support the implementation of required changes and… more
    CSL Behring (10/29/24)
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  • Senior Specialist, Financial Planning…

    Merck (North Wales, PA)
    …under the guidance of the Associate Director who supports the Global Regulatory Affairs & Clinical Safety (GRACS) and Quality Assurance (QA) organizations ... Provide financial planning, forecasting and analytical support to ourResearch&DevelopmentDivision, Global Regulatory Affairs & Clinical Safety (GRACS), and QA… more
    Merck (11/07/24)
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  • Senior Director , Head of Global…

    CSL Behring (King Of Prussia, PA)
    The Sr . Director , Head of Global Medical Information will oversee the global core functions of Medical Information across all therapeutic areas/products at CSL ... Clinical R&D, Pharmacovigilance, Quality, Marketing, Global Market Access/HCS, Heads of Medical Affairs in the US and International, TA Heads and global medical… more
    CSL Behring (10/25/24)
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  • Senior Principal Scientist, Clinical…

    Merck (North Wales, PA)
    …with talented and dedicated colleagues while developing and expanding your career. The Senior Director ( Sr . Principal Scientist) has primary responsibility ... placement, monitoring, analysis, regulatory reporting, and publication. Specifically, The Senior Director May Be Responsible For + Evaluating pre-clinical… more
    Merck (11/08/24)
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  • Associate Director , Marketing - HPV…

    Merck (North Wales, PA)
    …and resources to address the opportunities. + Collaborating with Global Medical and Scientific Affairs (GMSA), US, Senior Director of Medical Affairs ... **Job Description** **Job Description:** The Associate Director , Marketing, HPV Scientific Strategy plays a critical...One Company approach. + Collaborating with Program Leads, Medical Affairs and Global Expert Management & Strategy to plan… more
    Merck (11/09/24)
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  • Global Director Post Market Surveillance…

    Olympus Corporation of the Americas (Center Valley, PA)
    …Compliance Manager at 1-888-Olympus (###). Posting Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs (QA/RA) ... than @Olympus.com, it is likely not legitimate._ **Job Description** The Global Director of Post Market Surveillance Service Strategy & Programs is responsible for… more
    Olympus Corporation of the Americas (11/01/24)
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  • Director , Patient Advocacy, R&D

    J&J Family of Companies (Spring House, PA)
    …Development, Therapeutic Area Teams, Health Policy and Advocacy, Communications, Scientific Affairs , R&D, Senior Leadership) + Monitor the stakeholder ... Director , Patient Advocacy, R&D - 2406216492W **Description** Johnson...bioethics, legal, policy, and compliance. Externally, with patient organizations, regulatory bodies and other external stakeholders. The Patient Advocacy… more
    J&J Family of Companies (10/24/24)
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  • Principal Scientist ( Director ) - Women's…

    Merck (North Wales, PA)
    **Job Description** Under the guidance of a senior leader, the Principal Scientist, Outcomes Research-Women's Cancer has primary responsibility for developing value ... incumbent is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates and may… more
    Merck (11/08/24)
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  • Principal Scientist, Clinical Research, GYN…

    Merck (North Wales, PA)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may be… more
    Merck (11/08/24)
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  • Head, R&D Quality

    CSL Behring (King Of Prussia, PA)
    …manufacture and commercial launch. Interface with other disciplines including Global Regulatory Affairs , Project Management, Operations and Commercial Operations ... 3 sentences). The purpose of the position of Executive Director R&D Quality is to lead a dedicated team...is responsible for the leadership and co-ordination of all regulatory GxP inspections for the R&D teams and across… more
    CSL Behring (09/28/24)
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