• 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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  • Research Assistant - Oncology

    Vitalief (Newark, NJ)
    …documentation as applicable. + Enter, maintain, and reconcile study data in EDC , CTMS, and institutional systems (eg, OnCore, Epic, ClinicalTrials.gov) in a timely ... Microsoft Office.), with the ability to learn research-specific systems such as EDC , CTMS, and electronic health records. + Ability to follow established procedures,… more
    Vitalief (01/10/26)
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  • Senior Manager, Clinical Data Management

    Bristol Myers Squibb (Madison, NJ)
    …Takes a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (eCOA, ... practices regarding data management + Strong knowledge and experience of EDC systems (Medidata RAVE preferred); demonstrated knowledge of Microsoft Office skills… more
    Bristol Myers Squibb (01/09/26)
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  • New Brunswick, NJ - Clinical Research Coordinator

    Actalent (New Brunswick, NJ)
    …Responsibilities + Collect and enter data into the Electronic Data Capture ( EDC ) system + Resolve data queries efficiently + Communicate effectively about clinical ... Skills + Experience as a Clinical Research Coordinator + Minimum of 2 years of EDC data entry experience + Training in HIPAA and Good Clinical Practice (GCP) +… more
    Actalent (01/07/26)
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  • Part-Time Oncology Clinical Research Coordinator

    Actalent (New Brunswick, NJ)
    …a week. Responsibilities + Collect and enter data into the Electronic Data Capture ( EDC ) system. + Resolve queries related to clinical trial data. Essential Skills + ... years of oncology clinical trial experience. + Minimum of 2 years of experience in EDC data entry. + Training in HIPAA & GCP. Work Environment The position operates… more
    Actalent (01/06/26)
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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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  • Post Doctoral Research Associate

    New Jersey Institute of Technology (Newark, NJ)
    …Type: Staff Position Summary: The Endocrine Disruption and Chemical Biology Laboratory ( EDC Lab) is recruiting a Postdoctoral Research Assistant to join our team ... in Summer 2023. Our research bridges reproductive biology, toxicology, and sustainable chemistry to study the mechanisms by which environmental chemicals act as endocrine disruptors. Specifically, we combine chemical biology techniques with in vitro mouse… more
    New Jersey Institute of Technology (01/10/26)
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  • Senior Manager Clinical Study Lead (Cell Therapy)

    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 (01/09/26)
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  • Manager Database Management & Analytics, CSPV

    System One (Basking Ridge, NJ)
    …reporting, data migration, data integration, E2B Gateway reporting set-up, interface with EDC and other new automation initiatives. + Assists with data management of ... safety-related PV systems. + Other duties as assigned. + Must be available to work during US Business Hours Skills: + Experience supporting Oracle Argus Safety is required. + Experience in safety reporting applications is required. Knowledge of PV reports… more
    System One (01/08/26)
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  • Clinical Research Coordinator

    Actalent (Hoboken, NJ)
    …to detail. + Proficiency with clinical trial databases, IVR systems, and EDC . + Critical thinking and problem-solving abilities. + Positive attitude and high ... level of motivation. + Professional writing and communication skills. + Ability to work independently in a fast-paced environment. Additional Skills & Qualifications + Bachelor's Degree preferred or equivalent combination of education and experience. + Minimum… more
    Actalent (01/08/26)
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