• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and immune disorders. Job Summary:This position will be a member of the Risk Management Center of Excellence office who will help manage risk management ... Individual will provide strategic advice, teachings, and support related to risk management planning, risk management sciences, and risk management more
    HireLifeScience (05/23/24)
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  • Novo Nordisk Inc. (Stamford, CT)
    …strategies Implements proactive risk identification and mitigation planning for assigned clinical trial sites, leveraging Risk Based Quality Management (RBQM) ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...education and collecting data to support efficacy and new product development, CMR is involved. The one thing that… more
    HireLifeScience (05/14/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    Clinical sub-team and to drive the development and delivery of the clinical development plan in alignment with the product development strategy.Manages team ... immune disorders. Summary This position is responsible for providing project management , drug development expertise to Global Project Teams including strategic… more
    HireLifeScience (05/25/24)
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  • Merck & Co. (Rahway, NJ)
    …systems and database expertise. Familiarity with statistical analysis methods and clinical data management concepts.US and/or worldwide drug or vaccine ... Job DescriptionThe Associate Principal Programmer leads the statistical programming activities for multiple and/or large/complex late stage drug/vaccine clinical more
    HireLifeScience (05/25/24)
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  • Merck & Co. (Rahway, NJ)
    …development, aiding technology development, and supplying Active Pharmaceutical Ingredient (API) for clinical use and drug product development. This will involve ... the Operations Specialist include the following:The Operations Specialist role at the Associate Specialist level will serve as a process team member supporting the… more
    HireLifeScience (05/21/24)
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  • Merck & Co. (Rahway, NJ)
    …adhere to international GMP requirements and applicable guidance for the production of clinical GMP drug substance, drug product and packaged goods across all ... Language (include Requirements For Education, Experience And Skills)Job Description:The Associate Director Quality Assurance, Facilities, Validation & Automation will… more
    HireLifeScience (05/24/24)
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  • Merck & Co. (Rahway, NJ)
    …in and/or leads cross-divisional technical teams focusing on late-stage clinical process development, characterization, and/or technology transfer and validation ... as mentoring of junior staff in the execution of internal or management of external laboratory activities.Provides technical leadership in the interpretations of… more
    HireLifeScience (05/25/24)
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  • Merck & Co. (Rahway, NJ)
    …development and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process ... of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New Jersey research… more
    HireLifeScience (05/18/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    management required- CRO experience preferred- Strong knowledge of clinical trials preferred- Demonstrated ability to leverage digital data and analytics ... plans for specific categories under the direction of the head of category management , for the creation, execution, tracking of strategies. Includes working under a… more
    HireLifeScience (05/09/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders.Summary The Technology Management (mAb, Drug Substance, Drug Product , or New Modality) Lead ... is responsible for the management of technology transfer of the manufacturing processes of...of the manufacturing processes of (mAb, Drug Substance, Drug Product , or New Modality) for investigational and commercial drugs… more
    HireLifeScience (04/21/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …for is provided to cross-functional teams including but not limited to product clinical development team(s), HEOR, PRA, medical affairs, manufacturing and ... around rare diseases and immune disorders. Job Summary: The Global Brand Associate Director is accountable for supporting the development, integration, and execution… more
    HireLifeScience (05/20/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). This position ... those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data… more
    HireLifeScience (05/22/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …centered around rare diseases and immune disorders. SUMMARYThe Associate Director, Pharmacoepidemiology position provides epidemiologic, methodological, and analytic ... of epidemiologic studies, including real-word evidence (RWE), supporting senior management in various epidemiological activities.This position independently carries out… more
    HireLifeScience (04/04/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …other research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Oncology Value Access & Pricing will both develop and ... functions including but not limited to Commercial, Marketing, Medical, Clinical Development, Public & Government Affairs.Responsibilities- Lead the development of… more
    HireLifeScience (03/01/24)
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  • Associate Clinical Product

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …self. Become a **maker of possible** with us. **Responsibilities:** **Collaborate with Clinical Study team, Medical Affairs,** ** Product Mana** **gemen** **t** ... monitoring inbound shipments and cost accruals per study. + Maintain Study Product and Study Supply inventory using Inventory management database. (Must… more
    BD (Becton, Dickinson and Company) (03/21/24)
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  • Sr Clinical Research Associate

    ThermoFisher Scientific (New York, NY)
    …using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to ... a CRA._ **Discover Impactful Work:** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site… more
    ThermoFisher Scientific (05/02/24)
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  • Associate Mako Product Specialist

    Stryker (New York, NY)
    …by Fortune Magazine! Learn more about our award-winning organization by visiting stryker.com Associate Mako Product Specialist - New York, NY **Who we** **want** ... to surgeons** **. Change healthcare.** **Improve** **lives.** As an Associate Mako Product Specialist at Stryker, you...for all things related to the Mako, you'll provide clinical support to all end-users, offer guidance and assistance… more
    Stryker (03/02/24)
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  • Senior Clinical Site Lead - NY Metro/NJ

    Abbott (Manhattan, NY)
    clinical sites and other Abbott clinical staff (eg, operations management , study team, Site Contracts Associate ), as needed. **Manage all aspects of ... expert that provides support, mentoring and guidance to other clinical site management colleagues and supports key...a level that allows for appropriate collaboration with Abbott clinical staff, eg Site CRA, Site Contract Associate more
    Abbott (05/04/24)
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  • Sr Mgr, Clinical Drug Supply & Logistics

    Regeneron Pharmaceuticals (Armonk, NY)
    …Logistics** is responsible for providing oversight of individual or multiple clinical programs, forecasting Investigational Product (IP) supply requirements for ... overall clinical development plan. + Works with clinical drug supply management to determine resourcing...to establish these timelines. + Manages and oversees investigational product (IP) inventory strategy; advises supply management more
    Regeneron Pharmaceuticals (05/14/24)
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  • Clinical Study Manager (Hybrid)

    Stryker (Mahwah, NJ)
    …to work with health registries and large databases + Work in compliance with clinical process, regulations and data management + Ability to work independently on ... strategies to obtain information and support concerning medical devices undergoing clinical investigation, post market surveillance or marketed/ product use… more
    Stryker (04/18/24)
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