• 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
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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
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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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  • Syneos Health, Inc. (New York, NY)
    …by monitoring data and processes from a centralized location. This includes conducting remote monitoring of trial sites to verify compliance with regulatory ... Dedicated - Oncology + CNS (Home-Based - Connecticut) Updated: Yesterday Location: USA-NY- Remote Job ID: 25102535 Description CRA II - Sponsor Dedicated - Oncology… more
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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
    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 Director, Clinical Science

    Bristol Myers Squibb (Princeton, NJ)
    … development, the position is responsible for various aspects of ongoing clinical trial program-related activities within the relevant therapeutic area. These ... their personal lives. Read more: careers.bms.com/working-with-us . **Summary** The Associate Director of Clinical Science plays a...may be assigned. + Acquires and utilizes knowledge of clinical trial design to develop or oversee… more
    Bristol Myers Squibb (12/23/25)
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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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  • Associate Director, Oncology…

    Bristol Myers Squibb (Princeton, NJ)
    …your application should be directed to Chat with Ripley. R1597891 : Associate Director, Oncology Clinical Biomarker Asset Lead, Translational Development ... will offer the greatest possible benefit to patients. **Position Summary** The Clinical Biomarker Asset Lead role will be responsible for development and execution… more
    Bristol Myers Squibb (01/12/26)
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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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  • Associate Director, Biostatistics

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …As core study/project team member, provide statistical input in different perspective of the clinical trial conduct such as CRF review, IRT setting, DMC set up, ... products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of... clinical , statistical, and regulatory literature for current clinical trial results, regulatory trends and new… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Associate Director, IT

    System One (Princeton, NJ)
    Job Title: Associate Director of IT - Life Sciences/ Clinical Location: Princeton, NJ (Mostly remote with some onsite collaboration required - only EST ... Lead data reporting and BI efforts, including graphical dashboards to support clinical trial progress and operational KPIs + Ensure compliance with CFR Part… more
    System One (12/05/25)
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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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  • Associate Director, Established Brands

    Bristol Myers Squibb (Princeton, NJ)
    … Overview for Type II variation and coordinate expert reports. + Provide clinical trial expertise for existing evidence generation studies or health-authority ... Read more: careers.bms.com/working-with-us . **Position Summary:** The Established Brands Associate Director, Medical Affairs, is responsible for leading and… more
    Bristol Myers Squibb (01/12/26)
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