• Insmed Incorporated (New York, NY)
    …and Regional accounts.Provide timely, fair balanced, objective, scientific and evidence-based medical information , and education to health care customers within ... required, unless candidate has strong related experience.Other Pharmaceutical experience - Medical Information , Medical Strategy, Clinical management/trial… more
    HireLifeScience (12/13/24)
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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 ... areas centered around rare diseases and immune disorders. Summary: The Associate Director, Regulatory Affairs - Regulatory Project Management (RPM) provides planning… more
    HireLifeScience (01/06/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Associate Principal Scientist of Device Technology Assessment and Early Development will spearhead early-stage device technology evaluation and ... and commercialization.Provide strategic leadership in the early development of medical devices and drug-device combination products, aligning with the company's… more
    HireLifeScience (01/07/25)
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  • Merck & Co. (North Wales, PA)
    …(Hybrid work model is combination of in-office and work from home) The Associate Director Market Access will work closely with agency partners, internal brand ... This role will report to the Director, Oncology Market Access. The Associate Director Market Access will be responsible for supporting Brand products tactical… more
    HireLifeScience (12/14/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Associate Director, Global Oncology Communications , will support the creation and implementation of external communications strategies, plans and ... support late-stage oncology pipeline communications efforts including data milestones, medical congress activities, executive visibility, internal communications and social… more
    HireLifeScience (01/04/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma.Legend Biotech is seeking QA Batch Disposition Associate Manager as part of the Quality team based in Raritan, NJ. Role ... practices.Develop positive relationships with the QA team, Quality Control, Information Technology, maintenance, Manufacturing personnel, Technical Operations personnel, Human… more
    HireLifeScience (11/08/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Associate Director of Scientific Nomenclature and Reference Data is responsible for assigning accurate chemical nomenclature to small molecules ... data sourcesDemonstrating knowledge of company policies and procedures governing information disclosureChemical NomenclatureLeveraging knowledge of IUPAC and CAS nomenclature… more
    HireLifeScience (12/11/24)
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  • Genmab (Plainsboro, NJ)
    …be our best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director, Key Accounts will shape, implement, and execute Key Account brand ... Insights & Analytics, Sales, Sales Learning & Dev., Market Access, and Medical to implement site-of-care strategiesWork productively to lead through external agency… more
    HireLifeScience (12/21/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Associate Director, CMO Operation as part of the Global Manufacturing and Supply ... on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability,… more
    HireLifeScience (12/12/24)
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  • Merck & Co. (North Wales, PA)
    …solutions that help everyone to be more productive and enable innovation.The Information Technology team at our Company's R&D division (our Research & Development ... processes are integrated into the overall product development plan.-Communicate PV information to internal and external stakeholders, such as regulatory authorities,… more
    HireLifeScience (01/07/25)
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  • Merck & Co. (Rahway, NJ)
    …DFMEA).Cross-functional communication - communicating complex mechanical engineering information in layman's terms to facilitate cross-functional understanding ... and managing external vendors/research partners.Preferred Experience and Skills:Experience with medical device development with understanding of Design Controls (21… more
    HireLifeScience (01/08/25)
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  • Aequor (Salt Lake City, UT)
    …be considered for the role: 1. High School Diploma or equivalent 2. Information Management: Collect, assemble, and manage information for approval or rejection ... related duties or assignments. Responsible for collecting, assembling, and managing information and making appropriate decisions on approval or rejection for all… more
    HireLifeScience (01/08/25)
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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 ... agencies inquiries and other reporting requirements are met. Provides information to other internal departments where deemed appropriate.Develop project plans… more
    HireLifeScience (01/06/25)
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  • Merck & Co. (Rahway, NJ)
    …their knowledge of product and process development in the (bio)pharmaceutical and/or medical device industries to set tactical and strategic direction on programs ... development activities including engineering design, engineering analysis and testing, medical device design controls, risk management, test method/fixture development,… more
    HireLifeScience (12/20/24)
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  • Merck & Co. (Rahway, NJ)
    …robust scientific methodology, we collaborate to discover the next medical breakthrough.Our company's Sterile Product Development department is a multidisciplinary ... status, or other applicable legally protected characteristics. - For more information about personal rights under the US Equal Opportunity Employment laws,… more
    HireLifeScience (01/07/25)
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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 ... Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational Research, Research, Informatics Services, Project Management… more
    HireLifeScience (12/13/24)
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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 ... within the Daiichi Sankyo organization to obtain and/or provide information /data for regulatory filings.Review and interpret regulatory guidelinesContinuing Education:… more
    HireLifeScience (12/19/24)
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  • Merck & Co. (North Wales, PA)
    …to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human ... status, or other applicable legally protected characteristics. - For more information about personal rights under the US Equal Opportunity Employment laws,… more
    HireLifeScience (12/13/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionRole Summary The Hematology US Scientific Director, Medical Affairs (SDMA) is a regionally based position in our Company's Research Laboratories, US ... Medical Affairs. The role drives scientific excellence and optimizes...priorities. Along with the USMA Field Leaders (Executive Director (ED)/ Associate Vice President (AV)), the SDMA is responsible for… more
    HireLifeScience (01/08/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …integrity, and timelines for assigned studies and escalates issues to the Associate Director of Medical Coding to gain resolution. Functional Expertise:Study ... Reviews and submits DS Medical Coding synonym list update requests to the Associate Director of Medical Coding to ensure accuracy and consistency of the… more
    HireLifeScience (12/13/24)
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