• 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 ... drive our strategic priorities. The Director , Principal Scientist | Regulatory Affairs Liaison is responsible for development and implementation of… more
    Merck (10/31/24)
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  • Senior Principal Scientist (Senior Director

    Merck (North Wales, PA)
    …Description** We are seeking a Senior Director (Sr. Principal Scientist) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that ... **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs Liaison is responsible...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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  • Director , Regulatory Affairs

    Merck (North Wales, PA)
    **Job Description** The Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy ... global regulatory point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS. + Develops worldwide… more
    Merck (11/09/24)
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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 responsible ... 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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  • Medical Director , Surgical Reconstruction,…

    Integra LifeSciences (Princeton, NJ)
    …in the Marketing, Business Development, R&D/Process Technologies Clinical Operations, Strategy, Regulatory Affairs , Market Access, and other key functions, to ... and making headway to help improve outcomes. The Medical Director for the Surgical Reconstruction (SR) Franchise will be...day-to-day running of, and leadership for, the Medical Science Liaison (MSL) team. This role works closely with key… more
    Integra LifeSciences (09/30/24)
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  • International Medical Director

    Novo Nordisk (Plainsboro, NJ)
    …the Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal and ... to make a difference? The Position The International Medical Director serves as a subject matter expert for our...Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams to deliver and drive… more
    Novo Nordisk (10/17/24)
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  • Senior Medical Director

    Novo Nordisk (Plainsboro, NJ)
    …Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal ... to make a difference? The Position As Senior Medical Director for the novel modalities team, you will be...Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams to deliver and drive… more
    Novo Nordisk (11/13/24)
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  • Director Global Oncology Marketing Lung…

    Merck (North Wales, PA)
    …across a complex set of stakeholders, including research and development, medical affairs , regulatory affairs , market analytics, Promotional Review Team, ... **Job Description** We are currently recruiting for a ** Director Global Oncology Marketing** for Lung cancer for our Company's oncology business. The Global… more
    Merck (11/02/24)
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  • Director , Medical Safety Assessment…

    Bristol Myers Squibb (Princeton, NJ)
    …in their personal lives. Read more: careers.bms.com/working-with-us . ** Director , Medical Safety Assessment Physician (Immunology)** **Functional Area Description** ... of certain postmarketing commitments, and ensuring compliance with global regulatory requirements. **Position Summary** . Lead safety activities and benefit-risk… more
    Bristol Myers Squibb (11/13/24)
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  • Associate Director Project Management Oligo…

    WuXi AppTec (Plainsboro, NJ)
    …in TIDES drug development from discovery through clinical to commercial. Moreover, our Regulatory Affairs CMC team is experienced in preparing CMC dossiers to ... tools & techniques, then implements corrective measures. + Serves as liaison with client contacts, manages day-to-day communications and organizes project team… more
    WuXi AppTec (10/18/24)
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