• Allen Spolden (New Brunswick, NJ)
    New Brunswick, United States | Posted on 12/14/2023 The remote‑based Clinical Trial Associate (CTA) will perform tasks related to supporting operational ... to support clinical study activities as defined by the clinical trial operating model. Perform developmental tasks with oversight of CTA Manager.… more
    job goal (01/12/26)
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  • Allen Spolden (New Brunswick, NJ)
    New Brunswick, United States | Posted on 12/14/2023 The remote-based Clinical Trial Associate (CTA) will perform tasks related to supporting operational ... to support clinical study activities as defined by the clinical trial operating model. Perform developmental tasks with oversight of CTA Manager.… more
    job goal (01/12/26)
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  • Allen Spolden (New Brunswick, NJ)
    A clinical research organization is seeking a Remote Clinical Trial Associate to support operational strategy and execute clinical studies. ... Responsibilities include assisting with study startup, ensuring regulatory readiness, and collaborating with study teams and CROs. Candidates should have a Bachelor's degree and at least one year of experience in the pharmaceutical industry, along with strong… more
    job goal (01/12/26)
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  • Allen Spolden (New Brunswick, NJ)
    A leading pharmaceutical company is seeking a Clinical Trial Associate (CTA) to support operational strategies in clinical studies. This remote position ... and have over 3 years of experience in the pharmaceutical industry or clinical research. The role necessitates some travel as needed. Generous benefits and time… more
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  • Shionogi Inc. in (Florham Park, NJ)
    …of audits, inspections, and quality investigations. Responsibilities Provide quality oversight of clinical trial operations and PV to ensure GCP and GVP ... Overview The Associate Director, GCP/GVP Quality Assurance provides senior-level quality...clinical study teams and advisory to PV. Evaluate clinical trial documentation, processes, and study plans… more
    job goal (01/13/26)
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  • Regeneron Pharmaceuticals, Inc (Basking Ridge, NJ)
    …involved in research activities for innovative statistical methods and applications in clinical trial development as well as providing training to ... communication skills. Solid knowledge of statistical analysis methodologies, experimental and clinical trial design Expertise in statistical software Does this… more
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  • Hispanic Alliance for Career Enhancement (Rahway, NJ)
    …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. MS in Computer Science, Statistics, Applied Mathematics, ... related field plus 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent interpersonal… more
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  • The Association of Technology, Management and Applied… (Rahway, NJ)
    …Sciences, Engineering or related field plus 9 years of SAS programming experience in a clinical trial environment. MS in the same fields plus 7+ years of SAS ... programming experience in a clinical trial environment. Department Required Skills & Experience Excellent interpersonal, negotiation, and collaboration skills.… more
    job goal (01/13/26)
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  • Character Biosciences (Jersey City, NJ)
    …which Character's data is leveraged to inform and direct drug discovery and clinical trial design. You will have responsibility for determining and implementing ... development, disease progression predictive modeling, and analyses related to clinical trial design. Collaborative cross‑functional analyses with members… more
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  • Syneos Health, Inc. (New York, NY)
    …solutions organization built to accelerate customer success. We translate unique clinical , medical affairs and commercial insights into outcomes to address modern ... market realities. Our Clinical Development model brings the customer and the patient...and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is… more
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  • 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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  • 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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  • 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 Research Associate

    IQVIA (Parsippany, NJ)
    …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
    IQVIA (12/30/25)
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  • Clinical Research Associate , IQVIA…

    IQVIA (New York, NY)
    …bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key ... role in ensuring the successful execution of clinical trials. In this position, you will be responsible...essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File… more
    IQVIA (01/05/26)
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  • Associate General Counsel, Advertising…

    Mallinckrodt Pharmaceuticals (Bridgewater, NJ)
    …policies. Research & Development Support: + Provide legal counsel on clinical trial agreements, investigator-initiated studies, and collaborations with academic ... Job Title Associate General Counsel, Advertising & Promotion / Clinical Development Requisition JR000015569 Associate General Counsel, Advertising &… more
    Mallinckrodt Pharmaceuticals (01/03/26)
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  • Senior Manager, Clinical Data Management

    Bristol Myers Squibb (Madison, NJ)
    …projects + Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects + ... BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, ...functional study team members to ensure on-going review of trial data currency, quality and completeness + Represents DM… more
    Bristol Myers Squibb (01/09/26)
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  • Associate Director, Strategy & Insights,…

    ThermoFisher Scientific (Bridgewater, NJ)
    …patient recruitment strategies and the implementation of digital and decentralized clinical trial solutions. + Proven experience providing protocol review ... of Patient-First technology solutions, supporting future innovation and advancing patient-centric clinical trial methodologies. At Thermo Fisher Scientific, we… more
    ThermoFisher Scientific (12/18/25)
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  • Associate Principal Scientist, Statistical…

    Merck (Rahway, NJ)
    …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in Computer Science, Statistics, Applied Mathematics, ... plus 7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** + Excellent interpersonal skills… more
    Merck (12/02/25)
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  • Associate Director, Biostatistics

    Pfizer (New York, NY)
    …source data key efficacy variables and analyses. * Perform the analyses of clinical trial data, provide statistical interpretation of results, and collaborate on ... the reporting of clinical trial results to regulatory authorities and the scientific community by contributing to the clinical study reports, clinical more
    Pfizer (01/08/26)
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