• Merck & Co. (Rahway, NJ)
    …of country and site budgets. Development, negotiation and completion of Clinical Trial Research Agreements (CTRA).Oversees and tracks clinical ... quality standards and adverse event reporting requirements internally and externally.Our Clinical Research and Pharmacovigilance team push the boundaries of… more
    HireLifeScience (04/17/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, ... Experience Qualifications1 or More Years with BS. preferredExperience considered relevant includes clinical or basic research in a Pharmaceutical company, a… more
    HireLifeScience (03/09/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, ... or More Years with Bachelor of Science required- Experience considered relevant includes clinical or basic research in a Pharmaceutical company, a Medical… more
    HireLifeScience (04/11/24)
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  • Clinical Research Associate

    WuXi AppTec (Cranbury, NJ)
    …specified by project manager or supervisor, including but not limited to mentoring of Clinical Research Associate ( CRA ) I and II personnel. + ... **Overview** The Clinical Research Associate III...clinical monitoring and required reporting, including pre-study visits, site invitation visits, routine monitoring visits (both onsite and… more
    WuXi AppTec (03/02/24)
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  • Sr CRA Resource Associate

    J&J Family of Companies (Somerville, NJ)
    …May perform accompanied site visits to assess and ensure quality and efficiency of Clinical Research Associates | Support CRA Resource Leader US in the ... Resource Associate is responsible for supporting the CRA Resource Manager by coordinating and tracking...and high-quality deliverables | Provide guidance and advice to Clinical Research Associates on company procedures and… more
    J&J Family of Companies (04/16/24)
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  • Sr CRA /Principal CRA - Northeast

    ThermoFisher Scientific (Bridgewater, NJ)
    … trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, ... global Clinical Operations colleagues within our PPD(R) clinical research services provide end-to-end support for...Impactful Work:** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts… more
    ThermoFisher Scientific (03/21/24)
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  • Clinical Scientist, Oncology (Senior…

    Bristol Myers Squibb (Princeton, NJ)
    …team meetings + Submission of clinical documents to TMF + Development of site and CRA training materials and presentation at SIVs and Investigator meetings. ... with the protocol in collaboration with Data Management/Programming + Site -interface in collaboration with trial physician as point of...Life Sciences (MD, PhD with 0-2 years of prior clinical research experience, or PharmD, MS, RN… more
    Bristol Myers Squibb (04/17/24)
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  • Clinical Operations Manager

    Merck (Trenton, NJ)
    …of country and site budgets. Development, negotiation and completion of Clinical Trial Research Agreements (CTRA). + Oversees and tracks clinical ... quality standards and adverse event reporting requirements internally and externally. Our Clinical Research and Pharmacovigilance team push the boundaries of… more
    Merck (04/17/24)
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  • Clinical Research Scientist,…

    Bristol Myers Squibb (Princeton, NJ)
    …+ Conduct literature review + Submit clinical documents to TMF + Develop site and CRA training materials and present these at SIVs and Investigator meetings ... co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members +...Life Sciences (MD, PhD with 0-2 years of prior clinical research experience, or PharmD, MS, RN… more
    Bristol Myers Squibb (04/19/24)
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  • Manager , Site Contracts and Budget…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, ... Years with BS. preferred + Experience considered relevant includes clinical or basic research in a Pharmaceutical...company, Academic Research Organization (ARO) or Contract Research Organization (CRO). CRA experience preferred. +… more
    Daiichi Sankyo Inc. (03/09/24)
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  • Senior Study Manager - Cardiometabolic

    Merck (Rahway, NJ)
    **Job Description** Our Clinical Research and Pharmacovigilance team push...interim and close out visits + Experience as a CRA Manager , Lead CRA or ... the boundaries of global healthcare through research and innovation. Through clinical trials and...stakeholders (study team, subsidiary country teams, vendors, committees, investigators, site personnel, etc.) in support of clinical more
    Merck (04/18/24)
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  • Senior Study Associate

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, ... Bachelor of Science required - Experience considered relevant includes clinical or basic research in a Pharmaceutical...company, Academic Research Organization (ARO) or Contract Research Organization (CRO). CRA experience preferred -… more
    Daiichi Sankyo Inc. (04/11/24)
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