• Merck & Co. (Rahway, NJ)
    …provides a high degree of technical and project management responsibility. The Associate Director - Process/Facility Lead position will report to the Director , ... include the following:The process/facility lead role at the Associate Director level will serve as a technical mentor and...serve as a team member of the MACS Detailed Design Phase and will go on to support new… more
    HireLifeScience (09/18/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …centered around rare diseases and immune disorders. Summary The Associate Director , Program Management is a senior position responsible for effectively planning, ... wide range of functions in Daiichi Sankyo (DS). Reporting to the Sr. Director , Enterprise Program Management, this position requires a capable leader with strong… more
    HireLifeScience (09/19/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders.Summary The Associate Director of ERP Applications is responsible for overseeing and enhancing designated ... applications that support various business processes. This role encompasses overseeing design , configuration, testing, and deployment to ensure these systems operate… more
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …as other research areas centered around rare diseases and immune disorders. Director , Diagnostic Sciences Global Companion Diagnostics Job Summary The Director ... supplemental studies to support development of Dx devices under design control process. They will lead identification and selection...of Dx assays and partners and will contribute to design and execution of technical assessment of assays, vendors,… more
    HireLifeScience (09/19/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... the effective strategy, design , execution, and interpretation of Oncology clinical trials. Position...provide clinical input into the eCRF (Case Report Form) design , participate in the UAT (User Acceptance Testing) and… more
    HireLifeScience (09/19/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders. Summary The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... the effective strategy, design , execution, and interpretation of Oncology clinical trials. Position...provide clinical input into the eCRF (Case Report Form) design , participate in the UAT (User Acceptance Testing) and… more
    HireLifeScience (09/19/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …research areas centered around rare diseases and immune disorders. SummaryThe Associate Director , Consumer Marketing serves as the patient, brand and product subject ... monitor the success of product messaging, programs and promotional effort. The Associate Director is also responsible for a broad array of brand functions including… more
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …disorders. Summary A key part of the Global HR team, the Associate Director of Global HR Communications and Change Management will be responsible for developing ... the development and execution of strategic change communication plans. The Associate Director will contribute to the development of these plans and most importantly,… more
    HireLifeScience (09/19/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing Clinical ... include the development of Clinical Pharmacology and Modeling and Simulation plans, design and lead study teams to execute Clinical Pharmacology studies, conduct… more
    HireLifeScience (09/19/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Sankyo. As a trusted partner, provide oversight of technical and solutions architecture and design for the R&D IT portfolio and to ensure that partners receive the ... Informatics is a Solutions Architect who supports the planning & definition, acquisition, design & system build, and testing phases of systems development of global… more
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving ... compounds in Immunology. With a focus on late-stage development, the Clinical Director will manage the entire cycle of clinical development, including study … more
    HireLifeScience (09/14/24)
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  • Merck & Co. (Rahway, NJ)
    …Point, PA / Rahway, NJ is seeking a curious and collaborative Director to support our rapidly expanding cardiology respiratory, metabolism and ophthalmology ... pipeline.As a Director , you will serve as an expert QP2 representative...including, but not limited to dose selection, clinical trial design , and go/no-go decisionsCollaborate with other functional areas, as… more
    HireLifeScience (09/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …diseases and immune disorders. Summary Position leads complex studies in study design , statistical analysis and interpretation of results with some supervision. This ... report (CSR): Leads statistical activities for complex studies including study design , protocol development, CRF review, SAP development, analysis files development,… more
    HireLifeScience (09/19/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Job Summary: Oversees one or more trials of medium to high complexity in design and geographic scope. Such trials could be pivotal for submission; Prepares clinical ... and leads external advisory panels to advise on Phase 2 study strategy, design , and conduct; Interacts with KOLs for indication specific advice; Leads broad… more
    HireLifeScience (09/19/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Summary Oversees one or more trials of medium to high complexity in design and geographic scope. Such trials could be pivotal for submission; Prepares clinical ... and leads external advisory panels to advise on Phase 2 study strategy, design , and conduct; Interacts with KOLs for indication specific advice; Leads broad… more
    HireLifeScience (09/19/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …for medium complexity studies including contributing to development of optimal study design , independently develop and execute statistical analysis plan and helps in ... Leads statistical activities for medium complexity studies including study design , protocol development, CRF review, SAP development, analysis files development,… more
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  • Merck & Co. (Rahway, NJ)
    …with Study Manager on study deliverables.Participates in the set up and design during study start up (eg, database set up)Lead medical monitoring team ... clinical data/medical protocol deviations in collaboration with the Clinical Director .Builds talent and capabilities of direcUindirect team members through proactive… more
    HireLifeScience (09/17/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe HR Organizational Readiness, Associate Director is an experienced employee engagement, change management and internal communications professional ... requirements and needs.Partner with internal and external suppliers on strategy, design , communications, and interactive multimedia development as needed to best… more
    HireLifeScience (09/17/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …typically a single non-pivotal trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates ... as team member with AROs/CROs. Drafts development plans, protocol profiles, and sections of submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to… more
    HireLifeScience (09/19/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …external publications, and regulatory authority submissions (IMPD/IND) Responsible to design the audit framework globally for Research area, specifically GLP/GCLP ... studies.Partners with Audit and Compliance QA function to develop compliance and risk criteria, in order to assure compliance with regulations, standards and guidance such as ISO, CLIA, etc.Ensures that laboratories and / or vendors that are responsible for… more
    HireLifeScience (09/19/24)
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