• Senior Product Management Specialist

    Ford Motor Company (Trenton, NJ)
    …Ford's data landscape. You will bring to life our Enterprise Data Council ( EDC ) strategy, ensuring data is managed and leveraged as a strategic asset across ... 2. Operationalize and ensure the effectiveness of the Enterprise Data Council ( EDC ), acting as the central figure for its strategic implementation and day-to-day… more
    Ford Motor Company (12/10/25)
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  • Manager, R&D Applications

    Sumitomo Pharma (Trenton, NJ)
    …implementing, integration, and managing Medidata & Veeva clinical systems (eg CTMS, EDC etc.) in a regulated environment_** **Job Duties and Responsibilities** + ... business processes, requirements and technology systems supporting Clinical Trials (eg EDC , CTMS, ETMF, Payments etc.) + 7+ years of progressively increasing… more
    Sumitomo Pharma (11/15/25)
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  • Principal Clinical Data Systems Specialist…

    Stryker (Trenton, NJ)
    …to grant user and site access using Medidata Cloud Administration for Rave ( EDC and Modules), Coder, RTSM and MMI (Imaging). + Follow Stryker standard processes ... for global clinical trials + Hands-on experience with PMV clinical studies, including EDC design, CRF development, edit checks, and UAT + Strong knowledge of data… more
    Stryker (12/27/25)
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  • Canine Handler - Explosive Detection

    Enhanced Protection Services (Passaic, NJ)
    …Explosive Detection K9 Handler partners with a trained Explosive Detection Canine ( EDC ), or "K9", to conduct searches in/at assigned client sites, including ... corporate buildings, loading docks, delivery vehicles, open areas and/or other situations as needed. **RESPONSIBILITIES:** + Partner with a trained Explosive Detection K9 to conduct searches in/at assigned client sites, including corporate buildings, loading… more
    Enhanced Protection Services (12/28/25)
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  • Sr. Manager, Clinical Research Scientist

    Taiho Oncology (Princeton, NJ)
    …registration documents and publications. + Reviews and summarizes ongoing clinical data (from EDC and listings) to monitor the quality of the study, ensure clean ... data flow into the study database and compliance with the protocol. + Keeps the latest knowledge in clinical development through publications and scientific conferences and leverages the knowledge for designing and summarizing clinical studies. + Keeps Sr.… more
    Taiho Oncology (12/23/25)
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  • CT Clinical Study Manager

    Philips (Mercerville, NJ)
    …experience in clinical research execution in the medical device industry. Experience using EDC , CTMS, and eTMF systems is highly preferred. + Your skills include ... profound knowledge of clinical research process legislation and ICH-GCP guidelines. + You have a Bachelor's/master's degree or higher in Life Sciences or an equivalent field. + You must be able to successfully perform the following minimum Physical, Cognitive… more
    Philips (12/19/25)
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  • Associate Principal Scientist, Clinical Research…

    Merck (Rahway, NJ)
    …| Inclusion. + Design and organization of paper and Electronic Data Capture ( EDC ) clinical studies that meet scientific and regulatory requirements by the setting of ... objectives, budget, resources, timelines, and the study protocol/related documentation. + Provide overall leadership and support to the study team. + Identify and select Investigators, laboratories and/or CROs. + Apply for the necessary study permits and… more
    Merck (12/18/25)
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  • Programing Project Leader

    Sanofi Group (Morristown, NJ)
    …packages such as R, SPLUS, JMP. + Experience with an Electronic Data Capture ( EDC ), such as RAVE, Oracle Clinical. **Why Choose Us?** + Bring the miracles of ... science to life alongside a supportive, future-focused team. + Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally. + Enjoy a thoughtful, well-crafted rewards… more
    Sanofi Group (12/18/25)
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  • Senior Manager Clinical Study Lead…

    Regeneron Pharmaceuticals (Warren, NJ)
    …applications including (but not limited to) Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC + Extensive experience in global clinical trial operations with unique ... knowledge and skills to contribute to the development of protocols and key study documents + Knowledge of ICH/GCP and regulatory guidelines/directives + Advanced project management skills, cross-functional team leadership and organizational skills + Line… more
    Regeneron Pharmaceuticals (12/17/25)
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  • Associate Director, IT

    System One (Princeton, NJ)
    …+ Familiar with clinical systems and trial platforms such as CTMS, Medidata RAVE, EDC , and related tools + Strong understanding of CDISC standards, 21 CFR Part 11, ... GCP, and system validation. + Demonstrated ability in change management, org restructuring, and talent development. + Experience in hybrid IT environments, ideally supporting both government and commercial projects. + Excellent communication skills with both… more
    System One (12/05/25)
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