• Clinical Study Associate I

    Actalent (Basking Ridge, NJ)
    …propose remediation plans for issues. + Distribute key study documents to the CRO and vendors. + Provide clinical administrative support, including preparing ... Job Title: Clinical Study Associate IJob Description Assist in planning... trial management support to study teams and track CRO and vendor performance to ensure compliance with the… more
    Actalent (01/17/26)
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  • Sr. Study Manager, Clinical Operations

    Taiho Oncology (Princeton, NJ)
    …to develop processes and mitigation strategies for assigned studies. + Collaborate with Clinical Development and CRO on study-specific training for study team ... 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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  • Study Associate I, Clinical Operations

    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 ... impactful results. The leadership and support provided by our Clinical Operations team are the cornerstone of our success...KPIs and performs quality review of the eTMF (per CRO oversight plan) while collaborating with internal and … more
    Taiho Oncology (11/13/25)
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  • Sr. Director, Global Clinical Supply Chain,…

    Teva Pharmaceuticals (Parsippany, NJ)
    Sr. Director, Global Clinical Supply Chain, GCO ( Global Clinical Operations) Date: Jan 18, 2026 Location: Parsippany, United States, New Jersey, 07054 Company: ... with. **The opportunity** We are seeking an experienced Senior Director/Head, Global Clinical Supply Chain to lead end-to-end clinical supply operations across… more
    Teva Pharmaceuticals (11/22/25)
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  • Clinical Laboratory Study Manager - FSP

    Parexel (Trenton, NJ)
    …work closely with project managers (central and/or specialty labs) and lend expertise to clinical trial management (CTM) and CRO to ensure samples are collected ... applications **Knowledge and Experience** : 6 - 8 years clinical research experience with academic, CRO or...8 years clinical research experience with academic, CRO or pharmaceutical/biotech industry. We are seeking a professional… more
    Parexel (01/15/26)
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  • Senior Manager, Clinical Data Management

    Bristol Myers Squibb (Madison, NJ)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Functional Area Description** Clinical Data Management key focus is to ensure data quality, ... data types (eCRF and non eCRF) collected in BMS clinical trials from study start to database lock. **Position...coaching and quality oversight of junior Data Management Leads **FSP/ CRO /Vendor Oversight** + May act as core member of… more
    Bristol Myers Squibb (01/09/26)
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  • Manager, Clinical Operations, Monitoring…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    **Job** **Summary** The Manager, Clinical Operations works closely with the OPDC Monitoring Oversight Lead to manage monitoring oversight activities including ... managing Clinical Monitoring Consultants (CMC) contracted to perform monitoring oversight...oversight duties as well as escalating issues related to CRO monitoring quality. While focusing on quality and compliance,… more
    Otsuka America Pharmaceutical Inc. (01/09/26)
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  • Clinical Study Physician - Oncology - FSP

    Parexel (Trenton, NJ)
    **Parexel FSP has an exciting opportunity for a Clinical Study Physician. This is a fully remote role! Oncology experience needed** External Job Description The ... a critical global role that is created to take up medical responsibilities of clinical trials within Clinical Development & Operations by a qualified and… more
    Parexel (01/16/26)
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  • Manager Clinical Drug Supply & Logistics

    Regeneron Pharmaceuticals (Warren, NJ)
    …improvement initiatives. This role applies to internally sourced studies and/or CRO /Partnered studies. Collaborates and interacts with clinical trial managers, ... The **Manager, Clinical Drug Supply & Logistics** is responsible for...for forecasting Investigational Product (IP) supply requirements for multiple clinical trials and for managing the IP distribution process… more
    Regeneron Pharmaceuticals (01/15/26)
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  • Associate Director, Clinical Research…

    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 ... treatment and improving patients' lives. As an Associate Director, Clinical Research Scientist, you will play a pivotal role...for Site Initiation Visits and Investigator Meetings, vendor / CRO staff, in collaboration with the medical lead. +… more
    Taiho Oncology (01/15/26)
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