• 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 ... 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
    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)
    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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  • 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, ... 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
    job goal (01/13/26)
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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 &...days may vary by site or organization) and one remote day (Friday). Remote does not apply… more
    job goal (01/13/26)
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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 ... Officer, serve as the Subject Matter Expert (SME) and leader for Vitalief's clinical trial budgeting and coverage analysis outsourcing services. + Design,… more
    Vitalief (12/30/25)
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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 ... Skills:** Clinical Development, Clinical Research, Clinical Sciences, Clinical Trial Planning,...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
    Merck (01/10/26)
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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, Quality Risk Specialist

    Bristol Myers Squibb (Madison, NJ)
    …in their personal lives. Read more: careers.bms.com/working-with-us . Job Description The Associate Director, RBQM - HOCT, ICN will mainly be responsible for ... effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback loop to… more
    Bristol Myers Squibb (01/10/26)
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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, ... 7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
    Merck (12/02/25)
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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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  • Senior Director, Clinical Research,…

    Merck (Rahway, NJ)
    …Atherosclerosis, Cardiology Clinical Research, Cardiovascular Diseases, Clinical Development, Clinical Studies, Clinical Trial Designs, Clinical ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
    Merck (01/10/26)
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