• Novo Nordisk Inc. (Plainsboro, NJ)
    …RWD and IT teams, clinical teams, medical affairs, and customers to execute on the studies ie, develop study protocol, manage study conduct, deliver study ... education and collecting data to support efficacy and new product development, CMR is involved. The one thing that...ready to make a difference? The Position The Executive Director , Real World Evidence (RWE), is responsible for assuring… more
    HireLifeScience (03/18/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …for a living. Are you ready to make a difference? The Position Drive study management activities and manage cross-functional study team, external service ... a collaborative work culture, including direct partnership with the Operations Director (s) Stakeholder Management : Build strong internal and external… more
    HireLifeScience (03/27/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …feasibility reports. Reviews the study feasibility reports and propose new studies according to the product strategic plan.Evaluation of safety signals: Lead ... studies . This position provides epidemiologic expertise and advice for future studies in line with the product strategic analysis plan. In collaboration… more
    HireLifeScience (03/01/24)
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  • Eisai, Inc (Nutley, NJ)
    …on project teams. This involves providing valuable statistical input on observational studies , actively participating in the formulation of study designs and ... diverse data sources (eg, clinical trial data, patient registries, and observational studies ) to support study design and otcomes measured.Align the… more
    HireLifeScience (03/06/24)
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  • Legend Biotech USA, Inc. (Piscataway, NJ)
    …of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking (Sr.) Director , Cell Therapy as part of the US R&D team based in Piscataway, NJ. ... relevant industry experience in immunotherapy of cancer. 6+ years of management experience in building, leading teams successfully. Expertise in engineering,… more
    HireLifeScience (03/27/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …medical accountability and oversight for one or more clinical trials. Matrix management responsibilities across the internal and external network. Manages Phase 1-3 ... studies (depending on assignment) with demonstrated decision-making capabilities. Provides...questions and answers safety questions (dose modifications, discontinuations, and management of adverse events)May participate in Site Initiation Visit… more
    HireLifeScience (03/07/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …to or independently leads the design, preparation and analysis of epidemiologic studies , including real-word evidence (RWE), supporting senior management in ... centered around rare diseases and immune disorders. SUMMARYThe Associate Director , Pharmacoepidemiology position provides epidemiologic, methodological, and analytic support… more
    HireLifeScience (03/14/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and operational execution. This position effectively works independently, interacting with study and project teams, senior management , and outside advisors ... and vendors.ResponsibilitiesStudy Planning: Plans and designs studies consistently with product development and clinical development plans. Studies the… more
    HireLifeScience (03/01/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …plan-ning and project strategic documents, including NNI Evidence Generation Plans and Product Development Plans Clinical study management : Provide regional ... education and collecting data to support efficacy and new product development, CMR is involved. The one thing that...clinical expertise in design, implementation and monitoring of clinical studies (from Phase 1 to 4) in a team… more
    HireLifeScience (03/15/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionThe Oncology Regional Medical Scientific Director (RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in ... Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non- product areas of interest to the Company and replies to scientific… more
    HireLifeScience (03/08/24)
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  • Eisai, Inc (NJ)
    …of trial results, final study report conclusions and publications.Serve as study director for trials: Provide critical medical input into the lifecycle ... profile, we want to hear from you. The Medical Director , US Medical Affairs provides medical leadership for medical...area to provide strategic input for the development of product strategies and liaises with external stakeholders to solicit… more
    HireLifeScience (02/14/24)
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  • Insmed Incorporated (Bridgewater, NJ)
    …development and communication of HEOR evidence to demonstrate the value of Insmed's product (s). The Associate Director will work closely with HEOR team members ... HEOR research projects as a subject matter expert including burden of illness studies , patient evidence studies , medical claims and electronic health records… more
    HireLifeScience (03/12/24)
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  • Eisai, Inc (Nutley, NJ)
    …of trial results, final study report conclusions and publications. May serve as study director for trials. Provide critical medical input into the lifecycle ... Affairs Strategic Plans: Under the direction of the Global Senior Medical Director , work with key stakeholders, alliance counterparts, management , and functional… more
    HireLifeScience (01/25/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …well as other research areas centered around rare diseases and immune disorders.Summary The Director , Clinical Safety, will be a product safety lead or part of ... , and provide safety leadership including but not limited to clinical studies , post-marketing surveillance, signal detection and management , important safety… more
    HireLifeScience (03/01/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …areas centered around rare diseases and immune disorders.Summary The Senior Director , Global Oncology Medical Affairs is responsible for developing the Global ... of the activities in the GMA plan including Launch Readiness and Life Cycle Management for the assigned compound and will report into the Global Oncology Medical… more
    HireLifeScience (03/01/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …Provide strategic leadership for all statistical programming activity related to study , project and submission. Manage CRO to ensure high quality compound ... harmonization of programming processes supporting global submission.Responsibilities- Statistical Programming Management : Coordinates outsourced statistical programming of analysis data sets… more
    HireLifeScience (03/02/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …areas centered around rare diseases and immune disorders.Summary The Senior Director , Global Oncology Medical Affairs is responsible for developing the Global ... of the activities in the GMA plan including Launch Readiness and Life Cycle Management for the assigned compound and will report into the Global Oncology Medical… more
    HireLifeScience (02/23/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionRole Summary:The Global Senior Director Medical Affairs (GDMA) is responsible for driving execution of scientific & medical affairs plans for their ... (TA) in key countries and regions. They are impactful members of Product Development Team sub-teams and Global Human Health commercialization teams. They collaborate… more
    HireLifeScience (03/08/24)
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  • Merck & Co. (Rahway, NJ)
    …our products is developed and realized. Role Summary: The Executive Director , Scientific Affairs (EDSA) maximizes meaningful bi-directional scientific exchange with ... to improve outcomes for patients.The EDSA leads a large investigator-initiated studies program in partnership with late-stage development teams in Medical Affairs… more
    HireLifeScience (03/14/24)
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  • Insmed Incorporated (Bridgewater, NJ)
    …in New York™, and Best Workplaces for Millennials™ lists.OverviewThe Associate Director of Biostatistics is responsible for the statistical aspects for complex ... clinical trial(s) or indication product line. This role leads the protocol statistical section...line. This role leads the protocol statistical section development, study setup, execution, analysis, and reporting of clinical trials,… more
    HireLifeScience (03/12/24)
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