• Associate Director, Clinical…

    Vitalief (New Brunswick, NJ)
    …seeking a dynamic, strategic, and client-facing leader to build and lead our Clinical Trial Budgeting and Coverage Analysis Services. This role combines hands-on ... serve as the Subject Matter Expert (SME) and leader for Vitalief's clinical trial budgeting and coverage analysis outsourcing services. + Design, launch, and… more
    Vitalief (12/30/25)
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  • Trial Master File (TMF) Specialist Oncology

    Sumitomo Pharma (Trenton, NJ)
    …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable ... SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that… more
    Sumitomo Pharma (11/05/25)
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  • Associate Clinical Project Manager,…

    IQVIA (Parsippany, NJ)
    …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... and uphold GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within a role that is accountable for… more
    IQVIA (12/18/25)
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  • Senior Clinical Research Associate…

    Parexel (Trenton, NJ)
    …associated with the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring Responsibilities and Study ... **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is...quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
    Parexel (12/07/25)
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  • Clinical Study Associate Manager…

    Regeneron Pharmaceuticals (Warren, NJ)
    …the Clinical Study Lead (CSL) by taking responsibility for areas of clinical trial delivery. This role applies to internally sourced studies and studies ... The ** Associate Manager Clinical Study** (CSAM) role...maintenance of study systems including but not limited to Clinical Trial Management System (CTMS) and … more
    Regeneron Pharmaceuticals (01/15/26)
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  • Study Associate I, Clinical…

    Taiho Oncology (Princeton, NJ)
    …sciences is preferred. Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site management experience in the pharmaceutical, ... team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for operational study support...to multi-task and effectively prioritize in order to ensure clinical trial goals. + Recognize potential obstacles… more
    Taiho Oncology (11/13/25)
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  • Sr. Clinical Research Associate…

    Parexel (Trenton, NJ)
    …activities associated with the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:** + Ensure proper ... The Senior Clinical Research Associate (Sr. CRA) is...quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
    Parexel (12/11/25)
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  • Associate Director Clinical Supply…

    Regeneron Pharmaceuticals (Warren, NJ)
    …with robust documentation workflow and archival of documentation of IP supply activities provided to clinical trial teams for the Trial Master File. + Lead ... The ** Associate Director of Clinical Supply Operations**...+ Must have broad knowledge and cross-functional understanding of clinical trial methodology. + Working knowledge of… more
    Regeneron Pharmaceuticals (01/21/26)
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  • Associate Principal Scientist,…

    Merck (Rahway, NJ)
    …exposure to clinical drug development with emphasis on key elements of clinical trial planning, execution, data analysis and reporting of clinical ... 5 years. **Required Skills:** Clinical Development, Clinical Research, Clinical Sciences, Clinical Trial Planning, Clinical Trials, Clinical … more
    Merck (01/10/26)
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  • Clinical Study Associate I

    Actalent (Basking Ridge, NJ)
    …Standard Operating Procedures (SOPs), FDA regulations/EU Directive, and ICH guidelines. Provide clinical trial management support to study teams and track CRO ... Job Title: Clinical Study Associate IJob Description Assist...study meetings. + Coordinate with Regulatory Operations to post trial information on public forums. + Support the Fair… more
    Actalent (01/17/26)
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