• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …other research areas centered around rare diseases and immune disorders.Summary The Clinical Trial Information Disclosure Manager leads company operational ... and the WHO, IFPMA, and EFPIA-PhRMA principles. A member of the Global Clinical Trial Disclosure Platform and Operations Committee. Facilitates the company's… more
    HireLifeScience (06/07/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …to the timeline, budget and objectives set forth by the Study team. The Clinical Study Manager role is primarily a tactical study delivery role, reporting ... in accordance with DS standards. Act as the project manager of the clinical study team to...to the CRO, but includes ancillary vendors (eg translations, trial insurance, and central laboratory).Work closely and oversee CRO… more
    HireLifeScience (06/19/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics and share with study team, ... regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines.The Senior Clinical Study Manager will have routine interaction with key… more
    HireLifeScience (05/22/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in… more
    HireLifeScience (06/06/24)
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  • Manager Clinical Trial

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders. **Summary** The Clinical Trial Information Disclosure Manager leads company operational ... IFPMA, and EFPIA-PhRMA principles. A member of the Global Clinical Trial Disclosure Platform and Operations Committee....Operations Committee. + Act as the lead Data Sharing Coordinator from external sources and internal SMEs. + Ensure… more
    Daiichi Sankyo Inc. (06/08/24)
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  • Clinical Trial Specialist

    Vitalief (New Brunswick, NJ)
    …Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief: + ... patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance, data management. and other clinical trial activities for solid tumor, high… more
    Vitalief (04/17/24)
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  • Clinical Research Coordinator

    Vitalief (New Brunswick, NJ)
    …Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief: + ... Responsibilities: + Under the direct supervision of the Nurse Manager of Clinical Research Center (CRC), you...of experience in Clinical Research as a Clinical Research Coordinator , with experience in patient… more
    Vitalief (04/17/24)
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  • Clinical Study Manager

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …to the timeline, budget and objectives set forth by the Study team. The Clinical Study Manager role is primarily a tactical study delivery role, reporting ... in accordance with DS standards. Act as the project manager of the clinical study team to...to the CRO, but includes ancillary vendors (eg translations, trial insurance, and central laboratory). + Work closely and… more
    Daiichi Sankyo Inc. (06/16/24)
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  • Clinical Study Associate I

    Actalent (Basking Ridge, NJ)
    …and International Conference on Harmonization (ICH) guidelines. * Key focus is on providing clinical trial management support to study teams and tracking CRO and ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within... system, Clinical project management, cro, irb, clinical study, regulatory documents, clinical trial more
    Actalent (06/18/24)
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  • Sr. Clinical Study Associate

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in… more
    Daiichi Sankyo Inc. (06/06/24)
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  • Manager , Site Contracts and Budget…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in… more
    Daiichi Sankyo Inc. (04/26/24)
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