• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …disorders. Summary This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational ... leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). This position may serve as an ad hoc member of Global Project Team (GPT)… more
    HireLifeScience (02/23/24)
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  • Merck & Co. (Rahway, NJ)
    …Publishing (RPP) organization, which operates within the larger framework of Global Regulatory Affairs, Clinical Safety, and Pharmacovigilance (GRACS), ... plays a crucial role in guiding and advancing projects by translating global regulatory strategy into actionable plans at the asset level. This individual acts… more
    HireLifeScience (03/23/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure ... medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
    HireLifeScience (03/19/24)
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  • Merck & Co. (North Wales, PA)
    …/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US ... corporate standards and policies and business objectives.Actively- participate in labeling and global regulatory team meetings to ensure support for anticipated… more
    HireLifeScience (03/01/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
    HireLifeScience (03/28/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
    HireLifeScience (03/28/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …team in the Global Oncology Value, Access, and Pricing (GOVAP) department. The Associate Director , Global Oncology RWE Generation will report directly to ... as well as building and retaining institutional memory within Daiichi Sankyo. The Associate Director , Global Oncology RWE Generation will work in… more
    HireLifeScience (03/12/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionJoin our team as the Associate Director , Educational Engagement Innovation Accelerator and be at the forefront of revolutionizing medical ... meet the needs of HCPs to treat and care for their patients.As the Associate Director , Educational Engagement Innovation Accelerator, you will be a key… more
    HireLifeScience (03/27/24)
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  • Merck & Co. (Rahway, NJ)
    …and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical Development organization and ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
    HireLifeScience (03/26/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …Nordisk, you will have the opportunity to build a life-changing career in a global business environment. We encourage our employees to make the most of their talent. ... independently in order to accomplish objectives. Relationships Reports to the Director , Patient Support Programs Rare Disease. Key internal relationships include… more
    HireLifeScience (03/27/24)
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  • Merck & Co. (Millsboro, DE)
    Job DescriptionPosition Description: Associate Director - Site Digital Technology Lead The Site Digital Technology Lead is the representative for Global ... Manufacturing Practices, Computer Systems Assurance, track and trace, and other global regulatory requirements that impact IT and OT systems in Manufacturing,… more
    HireLifeScience (03/22/24)
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  • Eisai, Inc (Nutley, NJ)
    …If this is your profile, we want to hear from you. Job Summary The Associate Director , Global Medical Affairs will provide medical leadership for medical ... Essential Functions Medical Affairs Strategic Plans: Under the direction of the Global Senior Medical Director , work with key stakeholders, alliance… more
    HireLifeScience (01/25/24)
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  • Merck & Co. (Rahway, NJ)
    …a member of the Medical Device Combination Products Quality QMS group, the Associate Director , will participate in and/or lead various initiatives in support ... of our business processes, systems, and data. - The Associate Director will collaborate and interact with...for other Quality Programs, as assigned. Understands the evolving global health authority regulatory requirements and works… more
    HireLifeScience (03/16/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Associate Director , Clinical Supply Operations (CSO) within Global Clinical Supply (GCS) is responsible for supporting launch and ... processes, as well as business continuity.Key responsibilities of the Associate Director , Clinical Supply Operations include:Supporting the implementation… more
    HireLifeScience (03/15/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …to date- Support regulatory inspection related activities as required- Support Head, Global strategy and operations to develop and plan the Global QA ... people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...responsibility to collaborate with, and support the head of Global QA strategy and operations. In this position, the… more
    HireLifeScience (02/07/24)
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  • Merck & Co. (North Wales, PA)
    …studies.-Under the direction of the Program Lead, you will collaborate with global , cross- functional team-members including clinical directors and study managers to ... trial team.Collaborates with the Medical Writer on clinical/scientific and regulatory documents.Partners with Study Manager on study deliverables.Participates in the… more
    HireLifeScience (03/22/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans,… more
    HireLifeScience (03/21/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …areas centered around rare diseases and immune disorders. SUMMARYThe Associate Director , Pharmacoepidemiology position provides epidemiologic, methodological, ... medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
    HireLifeScience (03/14/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …as other research areas centered around rare diseases and immune disorders.Summary The Associate Director , RACMC Portfolio Products, will be responsible for ... medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
    HireLifeScience (03/01/24)
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  • Merck & Co. (North Wales, PA)
    …development).The HCP Strategy lead will work closely with the HIV US Commercial director as part of the overall brand marketing team and will report directly ... drive and align on decisions, including field sales, marketing operations, Legal, Regulatory , Medical, etc.Our US marketing team has adopted an Agile operating model… more
    HireLifeScience (03/19/24)
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