• Clinical Study Associate I

    Actalent (Basking Ridge, NJ)
    …CRO Oversight Monitoring (CROOM) visit output 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
    Actalent (06/18/24)
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  • Clinical Trial Associate

    Bristol Myers Squibb (Princeton, NJ)
    Clinical Trial Managers (CTMs) Clinical Trial Monitors (CTMos), Study Start -up Specialists, Site Contract Leads, Vendor Operations Managers, Regional ... procedural requirements necessary for US investigative trial sites to conduct clinical trials, with accountability of executing these activities from study startup… more
    Bristol Myers Squibb (06/23/24)
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  • Sr. Clinical Study Associate

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …concern 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. (06/06/24)
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  • Sr Clinical Research Associate

    ThermoFisher Scientific (New York, NY)
    …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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  • Clinical Trial Associate

    Bristol Myers Squibb (Princeton, NJ)
    …administrative and business activities related to the conduct of clinical trials (registrational and non- registrational /Investigator Sponsored Research Studies) ... with investigative sites from study start -up to study closure. **Key Responsibilities and Major Duties...and non-drug (Lab kits, ECG) importation to support study site + Complete all payment activities including preparing invoices,… more
    Bristol Myers Squibb (06/19/24)
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  • Clinical Study Associate Mgr…

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    …+ Reviews site level informed consents and other patient-facing study start -up materials + Oversees setting up and maintenance of study systems including but ... The **Assoc Manager Clinical Study** (CSAM) role supports the Clinical...+ Monitors recruitment and retention + Monitors progress for site activation and monitoring visits + Supports data quality… more
    Regeneron Pharmaceuticals (06/20/24)
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  • Clinical Study Manager, Clinical

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …ensure that the CRO-generated documents are created in a timely manner (communication plan, site monitoring plan, etc) ahead of study start . Oversee CRO study ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions in...primarily a tactical study delivery role, reporting into an Associate Director or above responsible for Operational Study Strategy.… more
    Daiichi Sankyo Inc. (06/16/24)
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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 (06/24/24)
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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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  • Associate Director - MACS Equipment…

    Merck (Rahway, NJ)
    …mission is to serve as PR&D's internal node for small molecule drug substance clinical manufacture, and as preferred site for first pilot of commercial small ... the MACS EDFE Leader include the following: The EDFE Leader role at the Associate Director level will serve as a technical mentor and process team member supporting… more
    Merck (06/12/24)
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  • Associate Director, Supplier Relationship…

    Bristol Myers Squibb (New Brunswick, NJ)
    …sites and CMOs. + Accountable for establishing and managing the technical transfer start -up and spend budgets for assigned manufacturing site and the associated ... impact + Manage inventory risk assessment process for inventory located at manufacturing site . Lead efforts to manage and execute risk mitigation plans. + Lead cross… more
    Bristol Myers Squibb (06/19/24)
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  • Regional Delivery Lead

    Bristol Myers Squibb (Princeton, NJ)
    …**Drives the clinical trial feasibility process and decision-making for country, site , and patient allocations on behalf of a region in collaboration with global ... and in their personal lives. Read more: careers.bms.com/working-with-us . **Position:** Associate Director, Regional Delivery Lead (RDL) **Position Summary:** **The … more
    Bristol Myers Squibb (06/24/24)
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