• US Director , Payor & Access…

    Merck (Honolulu, HI)
    …and key decision makers + Knowledge of national and society treatment guidelines, clinical research processes, FDA regulations, and Office of the Inspector ... **Job Description** **Role Summary:** + The US Director , Payor and Access Strategy Lead,...clinical experience to guide and direct FM HS strategy in alignment with organizational priorities and unmet needs… more
    Merck (11/07/24)
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  • Regional Medical Scientific Director

    Merck (Honolulu, HI)
    …questions about Company products. The work of a Regional Medical Scientific Director is aligned to: Scientific Exchange, Research , Scientific Congress Support, ... for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies. The Regional Medical Scientific Director serves… more
    Merck (10/25/24)
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  • Director , Regulatory Medical Writing (1…

    J&J Family of Companies (Honolulu, HI)
    …This individual will be responsible for long-term planning and translating the strategy into integrated plans for submission clinical components. This includes ... Director , Regulatory Medical Writing (1 of 4) -...will develop and maintain submission training materials specific to clinical content, training teams as needed; and promotes optimized… more
    J&J Family of Companies (11/07/24)
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  • Oncology Regional Medical Scientific…

    Merck (Honolulu, HI)
    …questions about company products. The work of an Regional Medical Scientific Director is aligned to: Scientific Exchange, Research , Scientific Congress Support, ... for approved, in-development, and active company-sponsored trials and/or investigator-sponsored research studies. The Regional Medical Scientific Director serves… more
    Merck (10/22/24)
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  • Oncology Regional Medical Scientific (Associate)…

    Merck (Honolulu, HI)
    …in the Company's Areas of Interest (AOI) for the Regional Medical Scientific Director 's specific therapeutic area Research : + Upon request from Scientific ... strategy , including field standard operating procedures (SOPs), Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities. **Preferred Experience… more
    Merck (10/30/24)
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  • Associate Director , Medical Writing…

    Takeda Pharmaceuticals (Honolulu, HI)
    …resolution). + Working knowledge of current global regulatory requirements/guidelines applicable to clinical research (eg, GCP). + Working knowledge of the ... therapies to patients worldwide. Join Takeda as a Associate Director Medical Writing where you will be responsible for...therapeutic area depending on the scope and stage of clinical development and may or may not have direct… more
    Takeda Pharmaceuticals (10/05/24)
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  • Associate Director , Medical Science…

    J&J Family of Companies (Honolulu, HI)
    …insights within the interventional cardiology space. * Strong understanding of clinical research methodologies, regulatory guidelines, and medical terminology. * ... key option leaders (KOLs) and healthcare professionals, providing scientific gaps in medical research and assist in defining Medical Affairs Strategy . You will… more
    J&J Family of Companies (11/06/24)
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  • Executive Director Scientific Affairs…

    Merck (Honolulu, HI)
    …exchange with the worldwide clinical and academic community to positively impact Research and Development (R&D) strategy for new medicines and to improve ... scientific/ clinical insights in support of our Company's R&D strategy + Sustains our Company's scientific credibility and fosters and develops relationships… more
    Merck (10/30/24)
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  • Director , Data & Development Operations

    J&J Family of Companies (Honolulu, HI)
    Director , Data & Development Operations - 2406220613W **Description** Johnson & Johnson is currently recruiting for a ** Director , Data & Development Operations** ... for R&D Quality and the establishment and execution of a Data Operations strategy and capability that encompasses all functions of R&D Quality including data and… more
    J&J Family of Companies (11/05/24)
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  • Associate Director , Nonclinical Regulatory…

    Takeda Pharmaceuticals (Honolulu, HI)
    …Safety Research and Evaluation) to recognize aims, align on strategy , define executable timelines, and agree upon content for nonclinical regulatory submissions. ... best of my knowledge. **Job Description** **About the role:** **Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology and Marketed… more
    Takeda Pharmaceuticals (09/19/24)
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  • Assoc Director , Field Medical Affairs…

    Regeneron Pharmaceuticals (HI)
    …enhances the value and appropriate use of Regeneron products. You will work on clinical research sites and investigators, and support of research activities ... As an Associate Director , Field Medical Affairs, you will play a...role are to ensure accurate exchange and distribution of clinical and scientific information relevant to in-line and pipeline… more
    Regeneron Pharmaceuticals (09/18/24)
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  • Global Medical Director , Allergy

    ThermoFisher Scientific (HI)
    …frequent trips to Uppsala, Sweden. **What will you do?** **Medical, Scientific and Clinical Strategy ** + Develop a comprehensive medical strategy to ... experienced individual to join our team as Global Medical Director , Allergy on the Medical and Scientific Affairs (MSA)...(IDD). This role is responsible for developing a global strategy to drive growth within the medical domain of… more
    ThermoFisher Scientific (09/27/24)
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  • Director , Product Management…

    HealthEdge Software Inc (Honolulu, HI)
    …include creating a high-level vision, defining product requirements, performing market research , and assisting in go-to-market strategy . You will also ... **Overview** ** Director , Product Management** **Position Overview:** We are seeking...fuel a digital transformation, reduce costs, and improve both clinical outcomes and the member experience. **Your Impact:** +… more
    HealthEdge Software Inc (09/21/24)
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  • Associate Director , CMC Regulatory Affairs

    J&J Family of Companies (Honolulu, HI)
    Associate Director , CMC Regulatory Affairs - 2406221330W **Description** Johnson & Johnson is recruiting for an Associate Director , CMC Regulatory Affairs. This ... about the country specific requirements needed to support IND/IMPD during clinical development as well as during marketing applications globally. **Key… more
    J&J Family of Companies (11/07/24)
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  • Business Development Director

    Cardinal Health (Honolulu, HI)
    …Manufacturing and Controls (CMC) Development + Nonclinical Development and Consulting + Clinical Development and Research + Medical Writing + Regulatory ... the business, strategic growth is organized into three primary channels: _regulatory strategy and consulting_ , _medical writing,_ and _medical publishing_ . The… more
    Cardinal Health (10/04/24)
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  • Executive Director , Global CRO…

    Norstella (Honolulu, HI)
    Executive Director , Global CRO & Professional Services Company: Citeline Location: Remote, United States Date Posted: Sep 25, 2024 Employment Type: Full Time Job ID: ... Citeline is one of the world's leading providers of data and intelligence on clinical trials, drug treatments, medical devices and what's new in the regulatory and… more
    Norstella (09/26/24)
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  • Manager, Clinical Programs - Navista

    Cardinal Health (Honolulu, HI)
    …programs and solutions to enhance Cardinal Health's clinician facing business. The Clinical Programs Manager manages the research , business cases, development, ... and multi-year program management roadmaps (in conjunction with the Director ) for a portfolio of patient centered clinical...programs, services or solutions based on market and customer research and in conjunction with the Director .… more
    Cardinal Health (08/30/24)
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  • Program Manager, Precision Medicine & Genomics

    Cardinal Health (Honolulu, HI)
    …solutions and services to enhance Cardinal Health's clinician facing business. The Clinical Programs Manager manages the research , business cases, development, ... ) for a portfolio of products and/or services (ie Precision Medicine, Genomics, Clinical Trials Research , etc) During annual operating plan meetings and similar… more
    Cardinal Health (08/27/24)
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  • Medical Science Liaison, Hematology, Texas

    Takeda Pharmaceuticals (Honolulu, HI)
    …guidelines, molecular pathways, mechanism of action Takeda Oncology products including clinical outcomes and research opportunities. + Formulate and keep ... research and may assist in identifying, evaluating, and screening qualified research sites for company sponsored clinical investigation. + Actively… more
    Takeda Pharmaceuticals (10/31/24)
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  • Medical Scientific Liaison, Solid Tumor - Denver,…

    Takeda Pharmaceuticals (Honolulu, HI)
    …guidelines, molecular pathways, mechanism of action Takeda Oncology products including clinical outcomes and research opportunities. + Formulate and keep ... research and may assist in identifying, evaluating, and screening qualified research sites for company sponsored clinical investigation + Actively… more
    Takeda Pharmaceuticals (10/12/24)
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