• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …centered around rare diseases and immune disorders. SummaryThis position supports safety monitoring and risk management activities, provides insights on current ... clinical practice and guidelines, reviews and provides written assessments...position supports a senior physician in evaluating and mitigating safety signals as they arise. Additionally, this position works… more
    HireLifeScience (05/14/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionWith support of Sr CRA/CRA Clinical Research Associate ) and/or CRA Manager, acts as primary site contact and site manager throughout all phases of ... with CRA Manager, CRM ( Clinical Research Manager, TA Head and CRD ( Clinical Research Director ) as needed.Works in partnership with GCTO (Global Clinical more
    HireLifeScience (05/18/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionWith support of Sr CRA ( Clinical Research Associate ) and/or CRA Manager, acts as primary site contact and site manager-throughout all phases of a ... with CRA-Manager, CRM ( Clinical Research Manager), TA Head and CRD ( Clinical Research Director ) as needed.-Works in partnership with GCTO (Global … more
    HireLifeScience (05/18/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …stud(ies).Ensures trial master file is complete and accurate for assigned stud(ies).If assigned, Associate Director , Clinical Operations may act as the Study ... regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and… more
    HireLifeScience (05/18/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core ... Data Sheets (CCDS) for assigned products. This position drives/leads the maintenance of global labeling and associated documents (including cartons and external packaging in the US) for assigned Daiichi Sankyo products. This position ensures that draft… more
    HireLifeScience (05/21/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …equal opportunity employer including veterans and people with disabilities. Summary The Associate Director , External Data Management, is accountable for the ... of External data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance, CROs and External Vendors… more
    HireLifeScience (04/20/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …areas centered around rare diseases and immune disorders. SUMMARYThe Associate Director , Pharmacoepidemiology position provides epidemiologic, methodological, ... journalsAssess clinical trial and/or other data sources to contextualize safety events for assigned product. Research natural history of disease to characterize… more
    HireLifeScience (04/04/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …develop programming submission strategy, perform integrated analysis of efficacy and safety , generate submission data package, create TLFs to support submission QAs, ... perform ad-hoc and exploratory analysis requested by clinical team, and support agency response or potential Advisory Committee Meeting- Develop DSI programming… more
    HireLifeScience (04/03/24)
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  • Insmed Incorporated (Bridgewater, NJ)
    …internal and external stakeholders (therapeutic areas, clinical pharmacology, clinical operations, non- clinical safety , contract research organizations ... for Millennials™ lists.OverviewWithin the Translational Bioanalytical Sciences (TBS) group of Clinical Development, the role focuses on LC-MS/MS of small and large… more
    HireLifeScience (04/23/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …while innovating for future capabilities. We regulate accounting, uphold workplace safety , manage our supply chain and sampling, support technology, provide ... independently in order to accomplish objectives. Relationships Reports to the Director , Patient Support Programs Rare Disease. Key internal relationships include… more
    HireLifeScience (04/18/24)
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  • Associate Director , Clinical

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …around rare diseases and immune disorders. **Summary** This position supports safety monitoring and risk management activities, provides insights on current ... clinical practice and guidelines, reviews and provides written assessments...position supports a senior physician in evaluating and mitigating safety signals as they arise. Additionally, this position works… more
    Daiichi Sankyo Inc. (05/15/24)
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  • Associate Director , Clinical

    Regeneron Pharmaceuticals (Tarrytown, NY)
    Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, ... scientific integrity and interpretation of study data of a clinical development program. The Associate Director...and GCP guidelines as well as applicable SOPs regarding clinical safety + Possesses proficient scientific expertise… more
    Regeneron Pharmaceuticals (04/24/24)
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  • Nursing Associate Director

    Mercy University (Dobbs Ferry, NY)
    Nursing Associate Director of Clinical Simulation Lab Print (https://www.schooljobs.com/careers/mercyedu/jobs/newprint/4377897) Apply  Nursing Associate ... Non-Union + Description + Benefits Job Posting Summary The Associate Director of the Clinical ...medical skills learning lab. Recent medical surgical experience. + Safety standards and practices used in lab/classroom settings. Education… more
    Mercy University (04/23/24)
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  • Associate Director , Clinical

    Regeneron Pharmaceuticals (Tarrytown, NY)
    The Associate Director , Clinical Scientist leads in the development, evaluation, planning and execution of hematology oncology clinical studies and ... on clinical studies and programs. May be responsible to manage one or more clinical scientists. As an Associate Director , a typical day may include the… more
    Regeneron Pharmaceuticals (04/24/24)
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  • Associate Medical Director

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …therapeutic area preferred, along with relevant industry experience. A minium of 2-3yr ( Associate Director ), 4-8yr ( Director ) prior industry experience or ... The Associate Medical Director works with their...ICH and GCP guidelines as well as SOPs regarding safety * Authors clinical sections of communications/documentation… more
    Regeneron Pharmaceuticals (04/24/24)
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  • Associate Director , Clinical

    J&J Family of Companies (Raritan, NJ)
    Associate Director , Clinical Project...day to day management of one or more global clinical studies, in compliance with department safety ... Scientist - 2406187180W **Description** Johnson & Johnson is currently seeking an Associate Director , Clinical Project Scientist to join the Oncology Global… more
    J&J Family of Companies (05/11/24)
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  • Associate Director , Clinical

    Memorial Sloan-Kettering Cancer Center (New York, NY)
    …in taking your career to the next level? We have an exciting opportunity for an Associate Director of Clinical Nutrition. You will be Responsible for all ... reports to improve the quality of patient care and safety . + Develop and implement Clinical Nutrition...care and safety . + Develop and implement Clinical Nutrition Evidence-based Practice Programs. + Ensure ongoing IRB… more
    Memorial Sloan-Kettering Cancer Center (05/15/24)
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  • Director Clinical Development

    Intra-Cellular Therapies, Inc (New York, NY)
    …national origin, protected veteran status, disability or any other legally protected status. Associate Director Clinical Development Base Salary range $175K ... respect in all we do, create and deliver. The Associate Director / Director Clinical ...as primary contact for medical communication to ensure medical safety within studies. Develop and maintain relationships with sites… more
    Intra-Cellular Therapies, Inc (03/18/24)
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  • Associate Director , Clinician,…

    Pfizer (Pearl River, NY)
    …into country feasibility. **Support study team** + With supervision of medical monitor ( director /Sr director ) provides clinical input to protocol/study team ... Contributes to medical review and interpretation of efficacy and safety data from clinical trials; this includes...+ Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts… more
    Pfizer (05/20/24)
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  • Senior Medical Director , Neurosciences,…

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety + With oversight from the GM&ES CDU TFA Primary Responsible, ... an assigned therapeutic candidate: Responsible for the analysis of clinical data, including safety monitoring, responsible for...academic clinical trials (10 years post fellowship clinical and research experience, associate or full… more
    Regeneron Pharmaceuticals (04/24/24)
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