• Novo Nordisk Inc. (Plainsboro, NJ)
    …and mitigation planning for assigned clinical trial sites Drives and tracks site activation and start -up activities with clinical trial sites to ... trials improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, IRBs, clinical research vendors). Manages relationships… more
    HireLifeScience (05/31/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …for operational planning and execution at the study level with responsibility for clinical study plan and execution (from planning start -up, conduct, reporting ... with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and...file is complete and accurate for assigned stud(ies).If assigned, Associate Director, Clinical Operations may act as… more
    HireLifeScience (05/18/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …activities in collaboration with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics and ... disorders. Summary The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to Good … more
    HireLifeScience (05/22/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …of concern and bring to supervisor's attention.Track study metrics such as site start -up, Investigator/ site performance, recruitment, regulatory documents, ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good … more
    HireLifeScience (03/09/24)
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  • Associate Director Clinical

    Bristol Myers Squibb (Trenton, NJ)
    …Other duties may be assigned. + Directs the operational oversight and execution of clinical site start -up, management and monitoring in accordance with ... RayzeBio aims to be the global leader in radiopharmaceuticals. **Summary** The Associate Director Clinical Site Operations provides strategic oversight,… more
    Bristol Myers Squibb (05/29/24)
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  • Sr Clinical Research Associate

    ThermoFisher Scientific (Bridgewater, NJ)
    …colleagues within our PPD(R) clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study ... **Discover Impactful Work:** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on- site visits… more
    ThermoFisher Scientific (05/02/24)
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  • Senior Manager, Clinical Data Management

    Bristol Myers Squibb (Princeton, NJ)
    …integrity & completeness of all data types (eCRF and non eCRF) collected in BMS clinical trials from study start to database Lock . **Position Summary / ... R&D pipeline . This role may report into Director, Clinical Data Management or Associate Director, ...out the highest potential of each of our colleagues. **On- site Protocol** BMS has a diverse occupancy structure that… more
    Bristol Myers Squibb (06/03/24)
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  • Assoc Mgr Clinical Study

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    …this role. The position can be based in Armonk, NY or Basking Ridge, NJ._ A Clinical Study Associate Manager (CSAM) role supports the Clinical Study Lead ... (CSL) by taking responsibility for areas of clinical trial delivery. This role applies to internally sourced...site level informed consents and other patient-facing study start -up materials + Oversees setting up and maintenance of… more
    Regeneron Pharmaceuticals (05/23/24)
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  • Sr Mgr, Clinical Drug Supply & Logistics

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    …effort for clinical supply management functionality. + Monitors and manages clinical supply activities through IRT from study start -up through study closure. ... compliant shipment and delivery to investigator sites. Works with Clinical Logistics Associate to complete this activity...+ Designs, reviews, and approves IP-related study tools (for clinical study teams and investigative site use),… more
    Regeneron Pharmaceuticals (05/14/24)
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  • Manager, Site Contracts and Budget…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …and bring to supervisor's attention. + Track study metrics such as site start -up, Investigator/ site performance, recruitment, regulatory documents, TMF ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good … more
    Daiichi Sankyo Inc. (04/26/24)
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  • Executive Associate II, Late Oncology

    Bristol Myers Squibb (Princeton, NJ)
    …. **Position Summary** Provides administrative support to the Executive Director, Clinical Development Team Leader, Late Oncology Team 1 as well as ... within appropriate timelines. + Perform diverse administrative duties in support of Clinical Development Team lead (CDTL) and Clinical Development Leads (CDLs)… more
    Bristol Myers Squibb (05/30/24)
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