• Director : Vaccine Drug Product…

    Merck (West Point, PA)
    …Our company is seeking a highly motivated candidate for the position of Director , Vaccine Drug Product Development. Vaccine Drug Product Development ... **Job Description** Our company is a global health care leader with a diversified portfolio...The Director will report to the Executive Director of Vaccine Drug Product Development, have… more
    Merck (01/08/25)
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  • Director , Global Head…

    Ascendis Pharma (Princeton, NJ)
    …offer a dynamic workplace for employees to grow and develop their skills. The Director , Global Head of Publication Planning is responsible for leading the ... Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe,...of Patients, Science, and Passion, we use our TransCon(R) drug development platform to fulfill our mission of developing… more
    Ascendis Pharma (12/20/24)
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  • Associate Director - Global

    Novo Nordisk (Plainsboro, NJ)
    …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions + Serve ... preferred + Minimum of 8 years total pharmaceutical/related industry experience in drug development required + Demonstrated knowledge of global regulatory… more
    Novo Nordisk (12/17/24)
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  • Director , Global Regulatory Leader…

    J&J Family of Companies (Raritan, NJ)
    Johnson & Johnson Innovative Medicine is recruiting for a Director , Global Regulatory Leader. This position can be located in Spring House, PA; Horsham, PA; ... people can reach their potential. At Johnson & Johnson, we all belong. The Director , Global Regulatory Leader, is responsible for global regulatory… more
    J&J Family of Companies (12/10/24)
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  • Associate Director , Global Labeling…

    Takeda Pharmaceuticals (Trenton, NJ)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the ... of labeling content and strategy of multiple assigned products in various stages of drug development, which may include one high complexity product and updates to or… more
    Takeda Pharmaceuticals (10/16/24)
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  • Global Medical Affairs Senior…

    Sanofi Group (Bridgewater, NJ)
    **Job Title:** Global Medical Affairs Senior Director , Rhinology and Gastroenterology **Location:** Cambridge, MA **About The Job** We are an innovative ... global healthcare company, committed to transforming the lives of...ideas and tactics to prioritize the best areas for clinical trial investment. + Collaborate with alliance partners at… more
    Sanofi Group (12/28/24)
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  • Director , Early Clinical

    Bristol Myers Squibb (Princeton, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . The Early Clinical Development function is part of a global scientific organization ... molecules, biomarkers, and mechanistic hypotheses in humans. The group drives early clinical strategy, and the design, execution, and interpretation of studies to… more
    Bristol Myers Squibb (12/06/24)
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  • Director , Global Evidence…

    Takeda Pharmaceuticals (Trenton, NJ)
    …is true to the best of my knowledge. **Job Description** **OBJECTIVES:** Global Evidence and Outcomes (GEO) contributes to the successful development and ... new and innovative therapies. Assigned to one or more global product(s), or as the lead for a disease...GEO, this role informs and contributes to product strategies, clinical development plans and leads the development and execution… more
    Takeda Pharmaceuticals (12/15/24)
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  • Director , Global Regulatory…

    Bristol Myers Squibb (Princeton, NJ)
    …through all stages of a products lifecycle. Members of the organization develop global regulatory CMC strategies and partners with key stakeholders to execute the ... Medical Information to build/maintain database to address external questions regarding drug products. **Position Summary / Objective** Oversee management of multiple… more
    Bristol Myers Squibb (11/27/24)
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  • Clinical Scientist Lead - Psychiatry…

    Bristol Myers Squibb (Princeton, NJ)
    …and/or Psychiatric** **Key Competency Requirements:** + Advanced knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations + ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Clinical Science Lead reports through the Clinical Science function which… more
    Bristol Myers Squibb (01/07/25)
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  • Sr. Director , Drug /Device…

    Merck (West Point, PA)
    **Job Description** The Senior Director of Device Product Stewardship will lead a department of up to 15-20 personnel overseeing technical support and product ... effective and statistically sound CAPA plans and issue resolution. The Senior Director will ensure stewards have the appropriate processes and playbooks, appropriate… more
    Merck (12/05/24)
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  • Director , Quantitative Pharmacology…

    Merck (West Point, PA)
    …regulatory expectations and shape, present and defend regulatory documents and submissions. The Director is a skilled quantitative drug developer, with a strong, ... aligned, quantitative and model-informed framework to impact strategies and decisions of drug development teams. Finally, the Director mentors or supervises… more
    Merck (12/19/24)
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  • International Medical Director

    Novo Nordisk (Plainsboro, NJ)
    …within the liver disease team working with MASH and/or ALD projects covering clinical drug development from preclinical assessment through Phase 1-4. In doing ... We are building a multi-talented team of physician scientist drug developers that works together to tackle key challenges...clinical development problems + Work with the larger Global Project Team to deliver excellent medical support for… more
    Novo Nordisk (10/17/24)
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  • Director , Quantitative Pharmacology…

    Merck (Trenton, NJ)
    …rapidly to changing situations/environment. + Knowledge in ophthalmology and/or cardiometabolic clinical drug development programs + Knowledge in modeling of ... small molecules, biologics and non-traditional therapeutics like peptides, novel biological The Director is a skilled quantitative drug developer, with a strong,… more
    Merck (12/19/24)
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  • Senior International Medical Director

    Novo Nordisk (Plainsboro, NJ)
    …Qualifications + MD or the international equivalent is required + 4+ years of clinical drug development experience from the pharmaceutical or biotech industry + ... or industry. In this role, the Senior International Medical Director will be the medical lead for clinical...clinical development program as medical lead and expert drug developer, providing input and guidance to both internal… more
    Novo Nordisk (12/10/24)
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  • Sr. Director , PV Medical Surveillance

    Taiho Oncology (Princeton, NJ)
    Sr. Director , PV Medical Surveillance Princeton, NJ, USA Req #378 Monday, July 15, 2024 Looking for a chance to make a meaningful difference in the oncology space? ... guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are… more
    Taiho Oncology (10/14/24)
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  • Director , Medical Affairs - NYC - Remote

    Merck (Trenton, NJ)
    …and Oncology Translational Studies Program (OTSP) research studies. **Upon request from Global Clinical Trial Operations (GCTO):** + Identify barriers to patient ... about any drug , vaccine, or biologic product._ Regional Medical Scientific Director _have no sales objectives or accountability for prescribing or sales of any… more
    Merck (12/19/24)
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  • Director , Quantitative Pharmacology…

    Merck (Trenton, NJ)
    …team in the role of Director . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects ... strategic elements of drug development. As a subject matter expert, the Director within the QP2-IO Group will work closely with teams of highly collaborative,… more
    Merck (11/26/24)
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  • Associate Director , Regulatory Affairs

    Sumitomo Pharma (Trenton, NJ)
    …for the position of **Associate Director , Regulatory Affairs** . The Associate Director is part of the Global Regulatory Affairs (GRA) team based in ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, … more
    Sumitomo Pharma (11/21/24)
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  • Executive Director , Cell Therapy…

    Bristol Myers Squibb (Princeton, NJ)
    …vectors, drug product intermediates, drug products, and finished labeled drug product. The Executive Director , Cell Therapy Quality, Analytical Science & ... quality is maintained through the testing and release process. + Supports clinical and commercial global regulatory filings and authors/ reviews/approves… more
    Bristol Myers Squibb (12/20/24)
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