• Novo Nordisk Inc. (Plainsboro, NJ)
    …Board meetings for a Therapeutic Area in certain instances, at the discretion of Executive Director of Medical Affairs . Assists the Senior Medical ... of the Novo Nordisk portfolio. Relationships This position reports directly to the Sr. Director , Medical Affairs and will assist the Vice President and Sr. … more
    HireLifeScience (09/20/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …as other research areas centered around rare diseases and immune disorders. SummaryThe Director , Global Oncology Medical Affairs , Evidence Generation role is ... partnership with Global Health Economics Outcomes Research partner.- As a member of Global Medical Affairs Team (GMAT, or Joint Medical Affairs Team for… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …other research areas centered around rare diseases and immune disorders.SummaryThe Senior Director , Global Oncology Medical Affairs , Evidence Generation role ... Integrated Evidence Plans (IEP) with the Alliance Partner.- As a member of Global Medical Affairs Team (GMAT, or Joint Medical Affairs Team for Alliance… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …as other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director , Global Medical Affairs (GMA) Oncology- Medical ... internal global medical education trainings to support regional medical affairs team needs.ResponsibilitiesEnsure high quality, scientifically sound Global… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... around rare diseases and immune disorders.Summary With the Head of Government Affairs & Public Policy, this position will help lead Daiichi Sankyo's engagement… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... or More Years in the pharmaceutical industry preferred4 or More Years in regulatory affairs , NDA, sNDA, BLA filing to FDA preferred Travel:Ability to travel up to… more
    HireLifeScience (10/10/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... the product's lifecycle and across different indications. Represent Global Regulatory Affairs on the GPT (Global Project Team), Daiichi Sankyo governance processes,… more
    HireLifeScience (10/01/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experience requiredExperience with ex-US labeling… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Years in the pharmaceutical industry preferred1 or More Years in regulatory affairs requiredExperience in (s)NDA/BLA filing to FDA preferred Travel Ability to travel… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help… more
    HireLifeScience (09/24/24)
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  • Merck & Co. (San Francisco, CA)
    Job DescriptionRole SummaryThe Cardiovascular & Metabolism Regional Medical Scientific Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and ... from SLs, including questions about Company products. The work of a Regional Medical Scientific Director is aligned to: Scientific Exchange, Research, Scientific… more
    HireLifeScience (10/25/24)
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  • Merck & Co. (Boston, MA)
    Job DescriptionOur Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ... candidates must reside in the assigned territory (Boston area).Role SummaryThe Oncology Regional Medical Scientific Director - Head & Neck Cancers/Melanoma is a… more
    HireLifeScience (10/22/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... variety of processes and projects for all of Legal & Corporate Affairs (LCA) including but not limited to: Vendor/Budget Management, Records Management, Litigation,… more
    HireLifeScience (09/24/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …of TA priorities and business needs. Relationships This position may report into the Field Director , Medical Affairs (or in smaller TA's directly into the TA ... SD works closely with the TA Leadership Team and Medical Director team to identify and execute...for scientific resources, communications, and training initiatives for the medical affairs team Serve on Clinical Trial… more
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …not only Clinical Data Science and Evidence (CDSE) but more broadly within Clinical, Medical and Regulatory, Market Access and Public Affairs , as well as ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...you ready to make a difference? The Position The Director - Epidemiology leads the development and execution of… more
    HireLifeScience (10/26/24)
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  • Merck & Co. (Rahway, NJ)
    …The incumbent is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates ... Under -the guidance of a senior leader, the Executive Director will be responsible for developing a value and...with clinical development, BARDS (Biostatistics and Research Decision Sciences), medical affairs , market access, commercial and key… more
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  • Merck & Co. (North Wales, PA)
    …the Director may be responsible for: Providing scientific and medical leadership for strategic alliances and Co-partnership opportunities.-Supporting the team in ... and dedicated colleagues while developing and expanding your career.The Clinical Director (Principal Scientist) has primary responsibility for the planning and… more
    HireLifeScience (10/07/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …Internal relationships include working with Headquarters, NA CMR including Clinical Trial Management, Medical Affairs , Regulatory Affairs and other NNI skill ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and… more
    HireLifeScience (10/09/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Executive Director , Device Quality & Regulatory will play a pivotal leadership role within the organization, overseeing the quality assurance and ... regulatory CMC for complex medical devices, including auto-injectors and other innovative drug delivery...regulations and industry trends affecting device quality and regulatory affairs .Strategic ContributionsServe as a key member of the device… more
    HireLifeScience (10/24/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Title - Director / Principal Scientist, Regulatory Compliance Department - Device Quality & Regulatory Brief Description of Position- This ... will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). The primary responsibility for this position is to… more
    HireLifeScience (10/25/24)
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