• Daiichi Sankyo, Inc. (Bernards, NJ)
    …and immune disorders. Summary This position supports the strategy for driving global Clinical Study Start -Up activities for PV Safety Operations. This ... clinical study safety reporting and activities.Global Clinical Study Start -Up Documentation: Reviews... protocols to ensure consistency in safety requirements across studies related to a similar compound. Develops and maintains… more
    HireLifeScience (10/15/24)
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  • Merck & Co. (Rahway, NJ)
    …and-submission and approval processes, and understanding of how these impact study start -up.-Ability to indirectly influence investigators, vendors, external ... CRD, the person is responsible for preparing, analyzing, negotiating, and revising Clinical Research related contracts and budgets through all phases of the contract… more
    HireLifeScience (10/26/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …for DS Programs / Studies .- Serve as the subject matter expert for Study Data Managers during the planning/ start -up, conduct and close-out of external data ... of External data in Daiichi Sankyo R&D collaborating with Clinical and Medical teams, Functional Stakeholders, (QCP, Clinical...support the collection of diverse external data types. Advises Study Data Manager on complex vendor management… more
    HireLifeScience (10/10/24)
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  • Manager , Clinical Study

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …and immune disorders. **Summary** This position supports the strategy for driving global Clinical Study Start -Up activities for PV Safety Operations. This ... study safety reporting and activities. + Global Clinical Study Start -Up Documentation: Reviews... protocols to ensure consistency in safety requirements across studies related to a similar compound. Develops and maintains… more
    Daiichi Sankyo Inc. (10/15/24)
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  • Clinical Study Manager

    Actalent (New York, NY)
    Job Title: Clinical Study Manager Job...in the planning and execution of clinical studies . You will develop a cross-functional, integrated study ... protocol are met. You will act as a project manager for the clinical study ...management and departmental training efforts. Hard Skills + Global Clinical Trial Management + Hematology + START more
    Actalent (10/22/24)
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  • Clinical Trial Manager

    Gilead Sciences, Inc. (Parsippany, NJ)
    …Manages all components of small clinical studies , including Phase I studies . + Manages actively clinical study budgets and exercises proactive ... study logistics and oversees/ develops clinical study plans for assigned clinical studies...+ Ability to manage any component of full cycle study management, from start -up to close-out. +… more
    Gilead Sciences, Inc. (10/29/24)
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  • Clinical Trial Manager

    Actalent (Parsippany Troy Hills, NJ)
    clinical study team in accordance with standards. + Act as the project manager of the clinical study team to liaise and coordinate with internal ... Job Title: Clinical Study ManagerJob Description The incumbent...be responsible for ensuring the delivery and execution of clinical studies in one or more geographic… more
    Actalent (10/30/24)
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  • Clinical Data Manager

    System One (Tarrytown, NY)
    …management tasks for assigned study . * Coordinates, leads and performs clinical data management activities for assigned studies in accordance with client's ... o Monitors data clean-up process performed by CROs from study start -up through data archiving. o Provides...related field. Experience: Minimum 7 Years, required. Phase 3 clinical studies experience highly preferred. System One,… more
    System One (10/24/24)
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  • Project Manager - Clinical Trials

    Hackensack Meridian Health (Hackensack, NJ)
    Clinical Research Nurses, Clinical Research Coordinators, Regulatory and Study Start -Up Specialists, Clinical Data Coordinators, Study ... including regulatory, finance, and contracts to ensure efficient, competitive, and timely study start -ups and initiations. + Continually reviews study more
    Hackensack Meridian Health (08/31/24)
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  • Clinical Program Manager

    IQVIA (Parsippany, NJ)
    …healthcare and patient treatment options around the world. As Senior Project Leader/ Clinical Program Manager you will liaise directly between IQVIA/sponsor ... are the Clinical Lead for site management, the Project Vendor Manager , the Project Management Analyst for project coordination, tracking and financial analysis,… more
    IQVIA (10/15/24)
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  • Clinical Program Manager (RN/NP…

    Mount Sinai Health System (New York, NY)
    …per specifications of the protocol; and monitors test results, as appropriate Documents clinical study and therapy in patient's chart and all other databases ... **Job Description** The Clinical Program Manager provides clinical...for the Nursing Staff regarding specific protocols. + Manage clinical trials portfolio and assure timely regulatory start more
    Mount Sinai Health System (08/15/24)
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  • Clinical Operations Manager

    Merck (Rahway, NJ)
    …and submission and approval processes, and understanding of how these impact study start -up. + Ability to indirectly influence investigators, vendors, external ... CRD, the person is responsible for preparing, analyzing, negotiating, and revising Clinical Research related contracts and budgets through all phases of the contract… more
    Merck (10/26/24)
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  • Clinical Trial Coordinator (CTC) - Remote

    Merck (Rahway, NJ)
    …for comprehensive trial and site administration. Under the oversight of the Clinical Trial Coordinator Manager , the person prepares, collates, distributes, and ... role will collaborate at the local level closely with Clinical Operations Manager (COM), Clinical ...start -up and submissions + Obtain, track and update study insurance certificates + Support preparation of submission package… more
    Merck (10/24/24)
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  • Data Manager

    System One (Tarrytown, NY)
    …management tasks for assigned study . * Coordinates, leads and performs clinical data management activities for assigned studies in accordance with client's ... Title: Clinical Data Manager Location: Remote Duration:...o Monitors data clean-up process performed by CROs from study start -up through data archiving. o Provides… more
    System One (10/24/24)
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  • Senior Manager , eCOA Management

    Bristol Myers Squibb (Madison, NJ)
    …instruments for clinical trials, facilitating the end-to-end process, and working with clinical study teams and vendors to meet study requirements. ... in their personal lives. Read more: careers.bms.com/working-with-us . **Senior Manager , eCOA (Electronic Clinical Outcome Assessment) Management** **Division:**… more
    Bristol Myers Squibb (10/15/24)
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  • Associate Director, Clinical Systems…

    Merck (Rahway, NJ)
    …and control tools is required. + Basic knowledge of Site Monitoring, Study Start up, Data Management, Pharmacovigilance, Essential Document Management, and ... Investigator/ Study Coordinator roles/ responsibilities. + Experience with critical clinical systems such as CTMS, eTMF, Electronic Data Capture (EDC) system, … more
    Merck (10/23/24)
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  • Clinical Account Executive - Express…

    The Cigna Group (Morris Plains, NJ)
    **JOB DESCRIPTION** The Clinical Account Executive (CAE) position is an exciting opportunity for a pharmacist who is looking to leverage their pharmacy and ... the Health Plan client's strategic goals and drive improved clinical and financial outcomes for their membership. In this...Acts in concert with assigned Account Executive and Account Manager to service the health management consultative needs of… more
    The Cigna Group (10/30/24)
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  • Senior Manager , Companion Diagnostics…

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    …Development Program and Study Team Involvement:** + Serve as an active member of clinical study teams to ensure Dx/CDx planning is in line with clinical ... The role of Senior Manager , Diagnostics Program Management & Operational Delivery, is...the Dx/CDx strategy in parallel to the corresponding Regeneron clinical drug development programs and studies with… more
    Regeneron Pharmaceuticals (09/24/24)
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  • Principal Biostatistician, Early Phase

    IQVIA (New York, NY)
    …and takes proactive approach to gain efficiencies in work across protocols. + Study Start up: Assist with protocol development, sample size calculation, protocol ... + Leadership: Perform statistical team lead role on single studies . Through this, works closely with the Project Team...May be expected to present at bid defenses. + Clinical Study Report (CSR): Reviews or drafts… more
    IQVIA (09/24/24)
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