• Manager , Clinical Research

    Edwards Lifesciences (Trenton, NJ)
    …subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good ... skills. + Providing input on strategic direction on field monitoring of studies and data collection for clinical...cardiology trials + Master's Degree in related field + Clinical research certification (ACRP or SoCRA … more
    Edwards Lifesciences (12/18/25)
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  • Sr. Manager , Clinical

    Taiho Oncology (Princeton, NJ)
    …transforming the landscape of cancer treatment and improving patients' lives. As a Senior Manager , Clinical Research Scientist, you will play a pivotal role ... of cancer research . Position Summary: The Senior Manager , Clinical Research Scientist has...execution of key tasks involved in the design, conduct, monitoring and review of study data, analysis and reporting… more
    Taiho Oncology (12/23/25)
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  • Senior Clinical Research Associate/…

    Parexel (Trenton, NJ)
    …Specialist, Clinical Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience: Minimum 3 years ... (DSMM) + Partners with SCP and Country Study Operations Manager (SOM) + When required Partners with other Study...relevant experience in clinical research site monitoring (preferably 2 years in… more
    Parexel (12/07/25)
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  • Sr. Clinical Research Associate…

    Parexel (Trenton, NJ)
    …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the ... delivery of the study. The CRA is responsible for the preparation, initiation, monitoring , and closure of assigned sites in clinical studies, in compliance… more
    Parexel (12/10/25)
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  • Senior Clinical Research Associate…

    Parexel (Trenton, NJ)
    The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the ... delivery of the study. The SrCRA is responsible for the preparation, initiation, monitoring , and closure of assigned sites in clinical studies, in compliance… more
    Parexel (12/03/25)
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  • Central Monitoring , Manager

    Parexel (Trenton, NJ)
    The Manager , Central Monitoring is accountable for centralized monitoring activities for global and/or complex trials, analytical data review of key risk ... data and presenting as an integral member of the Clinical Study team for clinical development studies....interpreted, reported and presented to the study teams. The Manager , Central Monitoring , will be responsible for… more
    Parexel (12/20/25)
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  • Clinical Quality Operations Manager

    Merck (Trenton, NJ)
    …or business management is preferred. **Prerequisites:** + Minimum of 6 years in clinical research including at least 2 years with developing and managing ... up of regulatory inspections. **Operational Quality Management:** + The Clinical Quality Operations Manager is accountable for... Clinical Data Management, Clinical Development, Clinical Quality Management, Clinical Research ,… more
    Merck (12/15/25)
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  • Sr. Study Manager , Clinical

    Taiho Oncology (Princeton, NJ)
    …Under minimal supervision, leads and manages complex global studies to support the Clinical Development Plan. The Senior Study Manager (SSM) is responsible for ... and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources… more
    Taiho Oncology (11/13/25)
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  • Senior Manager , Global Quality Management…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …sciences or related field; advanced degree a plus. + 6-8 years of experience in clinical quality assurance or clinical research within the pharmaceutical or ... **Job Summary** The Senior Manager of Global Quality Management (GQM) supports the...of Global Quality Management (GQM) supports the execution of clinical quality activities to ensure compliance with Good … more
    Otsuka America Pharmaceutical Inc. (12/16/25)
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  • Senior Clinical Trial Physician/…

    Bristol Myers Squibb (Princeton, NJ)
    …in order to gain their inputs on emerging science in drug and biomarker research , disease knowledge, and design of clinical development studies and programs * ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Clinical Trial Physician sits within Clinical Development, which is a… more
    Bristol Myers Squibb (12/21/25)
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  • Senior Clinical Scientist, Oncology

    Bristol Myers Squibb (Princeton, NJ)
    …other scientific field preferred) **Experience Requirements** + 5+ years of experience in clinical science, clinical research , or equivalent + Proficient ... and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Clinical Scientist reports through the Clinical Science function which… more
    Bristol Myers Squibb (12/09/25)
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  • Feasibility Study Manager

    Parexel (Trenton, NJ)
    …or equivalent. + **Experience:** 3-5 years of relevant industry experience ( clinical research , feasibility, site engagement, project coordination, or related ... **PXL FSP - Join an organization shaping smarter, faster clinical development** PXL FSP is seeking a detail‑oriented and proactive **Feasibility Study Manager **… more
    Parexel (12/19/25)
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  • Senior Manager , State & Local Income Tax

    Bristol Myers Squibb (Princeton, NJ)
    …local tax returns, management of state notices and audit inquiries, tax technical research and analysis, monitoring tax legislation and state tax audit support, ... work and in their personal lives. Read more: careers.bms.com/working-with-us . As a Senior Manager , State and Local Tax Compliance you will be a critical member of… more
    Bristol Myers Squibb (12/03/25)
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  • Sr. Manager , PV Sciences

    Taiho Oncology (Princeton, NJ)
    …and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources ... Proposition: Embark on a transformative journey with Taiho Oncology as a Senior Manager in PV Sciences. At the forefront of pharmacovigilance innovation, we offer a… more
    Taiho Oncology (12/13/25)
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  • Manager , PVRM

    Sumitomo Pharma (Trenton, NJ)
    …diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For more ... across the SMPA organization including, but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and… more
    Sumitomo Pharma (10/30/25)
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  • Senior Manager , Engineering & Applied…

    Oracle (Trenton, NJ)
    …of sophisticated Retrieval-Augmented Generation (RAG) systems. + Collaborate with product management, research , and clinical teams to define and execute the ... to create something world-class from the ground up. We're seeking a **Senior Manager of Engineering & Applied Scientists** -a hands-on technology leader who thrives… more
    Oracle (12/22/25)
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  • Sr. Manager , Procurement, Portfolio…

    Bristol Myers Squibb (Princeton, NJ)
    …operational, and data-informed decision support to the CDP ( Clinical Development Procurement) Leadership Team-coordinating priorities, tracking execution, and ... Head of CD Procurement translating strategy into clear execution plans, monitoring progress, and enabling continuous improvement across projects and governance… more
    Bristol Myers Squibb (12/06/25)
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  • Associate / Medical Director - Rheumatology…

    Parexel (Trenton, NJ)
    …Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to travel 15-20% is required _**Internal ... + Participate in the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated clinical and… more
    Parexel (10/11/25)
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  • Senior Physician, Patient Safety (Senior Drug…

    Parexel (Trenton, NJ)
    …processing cycle + Provide input as necessary to Feasibility Studies, Data Monitoring Committees (DMCs), Clinical Endpoint Committees (CECs) + Provide medical ... + Perform review and summarization of literature citations including epidemiology background research + Provide safety content review of clinical protocols,… more
    Parexel (12/06/25)
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  • Full-Time, Temporary Registered Nurse

    The Center for Great Expectations (Somerset, NJ)
    …and training set forth by Human Resources. 8.) Actively participate in CGE's clinical research efforts by ensuring accurate and timely reporting for all ... set forth in NJAC 10:161A-1.5. + Coordinate infant care and wellness with Clinical staff and Program Manager . + Participate in weekly multidisciplinary team… more
    The Center for Great Expectations (12/03/25)
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