• Genmab (Plainsboro, NJ)
    …and authentic is essential to fulfilling our purpose.The RoleGenmab is searching for an experienced Director , Global Clinical Drug Supply to be part of ... at the forefront of bringing medicines to cancer patients and other serious diseases. Director , Global Clinical Drug Supply will work in partnership with… more
    HireLifeScience (01/07/25)
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  • Genmab (Plainsboro, NJ)
    …collaboration, excellence, and a can-do attitude to achieve results.You will be reporting to Director , Global Clinical Drug Supply in Copenhagen, ... an experienced Senior Clinical Drug Supply Manager to join our Global Clinical Drug Supply Operations team.As Senior Clinical Drug Supply… more
    HireLifeScience (12/19/24)
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  • Merck & Co. (Rahway, NJ)
    …a particular focus on obesity and obesity-related metabolic disorders. - The Senior Director will manage the entire cycle of clinical development, including ... monitoring, analysis, regulatory reporting, and publication. - Specifically, the Senior Director may be responsible for Evaluating pre- clinical and translational… more
    HireLifeScience (01/25/25)
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  • Merck & Co. (Rahway, NJ)
    …medicines. Our Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of ... decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication;...study of marketed compounds. In executing these duties, the Director may: Supervise the activities of Clinical more
    HireLifeScience (01/16/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Global Clinical Supply organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full company ... Research Laboratories portfolio of clinical trials.- Global Clinical Supply...the timelines for bulk manufacturing needs and release of drug product across assigned program(s).-Works directly in the SAP… more
    HireLifeScience (01/16/25)
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  • Merck & Co. (Rahway, 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
    HireLifeScience (01/25/25)
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  • Merck & Co. (Rahway, NJ)
    …degree (eg, MS, MBA, Ph.D., PharmD) preferred - Experience and knowledge of clinical drug development strongly preferred; including the different phases of ... drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in...our company. - Position Description/Summary: - The GPAM Associate Director , Project Manager, is a core member of Early… more
    HireLifeScience (01/03/25)
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  • Merck & Co. (Rahway, NJ)
    …in the role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects ... registration. Associate Directors are emerging leaders in the field of quantitative drug development, with a developing understanding of the strategic elements of … more
    HireLifeScience (01/25/25)
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  • Merck & Co. (Rahway, NJ)
    …and inclusive work environment.Essential Knowledge, Duties & Responsibilities for the Director Include:Sterile drug product development concepts, tools, and ... Job DescriptionOur Company is a global health care leader with a diversified portfolio...for the research and development of sterile & parenteral drug products for biologics including monoclonal antibodies (mAbs), di-… more
    HireLifeScience (01/23/25)
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  • Merck & Co. (Rahway, NJ)
    clinical trial design and Go/No Go decisionsFraming critical drug development questions for optimizing model-informed development-Responsible for developing and ... DescriptionThe Quantitative Pharmacology and Pharmacometrics (QP2) department drive model-informed drug discovery and development (MIDD) to routinely enable efficient… more
    HireLifeScience (01/24/25)
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  • Merck & Co. (Rahway, NJ)
    …Our company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of ... placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May Be Responsible ForEvaluating pre- clinical and… more
    HireLifeScience (01/25/25)
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  • Merck & Co. (Rahway, NJ)
    …Scientist (Executive Director ) and Product Development Team (PDT) lead, Oncology Global Clinical Development, has primary responsibility for the planning and ... /PDT lead may:-Manage Directors and/or Senior Directors responsible for Oncology Global Clinical Development projects.-Supervise the activities of entire … more
    HireLifeScience (01/25/25)
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  • Merck & Co. (Rahway, NJ)
    …approach, driving the development of in vitro-in vivo relationships and preclinical-to- clinical translation in bioperformance of formulationsThe Director will ... Job DescriptionOur company is a global health care leader with a diversified portfolio...for the research and development of sterile & parenteral drug products for biologics as well as the biopharmaceutics… more
    HireLifeScience (01/03/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionR5 - Director - Pharmacometrics, Quantitative Pharmacology and PharmacometricsT he (remote) position is only applicable for those that are not within ... than) The Quantitative Pharmacology and Pharmacometrics (QP2) department drives model-informed drug discovery and development (MIDD) to routinely enable efficient … more
    HireLifeScience (01/11/25)
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  • Merck & Co. (Rahway, NJ)
    …to ensure they have a medical contact within the company.Upon request from Global Clinical Trial Operations (GCTO), support Company-Sponsored Trials to enhance ... qualifications for a specific compound or trial.Recommend potential study sites to Global Clinical Trial Operations (GCTO)/ Clinical Research.Address requests… more
    HireLifeScience (01/10/25)
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  • Merck & Co. (Rahway, NJ)
    …Our company's oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of ... design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may be responsible for: -Evaluating pre- clinical and… more
    HireLifeScience (01/16/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …when needed Clinical Development Expertise Strategy:In collaboration with the Global Clinical Lead (GCL), if applicable, leads the development and ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
    HireLifeScience (01/17/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    Director , Clinical Study Startup to establish the strategy driving global Clinical Study Start-Up activities for PV Safety Operations. This position ... make decisions where appropriate and escalate any complex problems to the Director , Clinical Study Startup.This position requires strong organization and… more
    HireLifeScience (01/06/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …as a project manager/leader in planning and executing strategies for global drug development, commercialization and life cycle management. preferredProven ... Summary This position is responsible for providing project management, drug development expertise to Global Project Teams...these objectives. This position will report to the Sr Director , Group Leader, GPM&L or the Executive Director more
    HireLifeScience (01/10/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... and immune disorders. Summary: Responsible for leading and developing global regulatory strategy for assigned development projects. Represents Daiichi Sankyo's… more
    HireLifeScience (12/18/24)
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