• Administrative Services Coordinator CPUP…

    Penn Medicine (Philadelphia, PA)
    …enrolled in these studies. * Schedule follow up studies as directed by the trial protocol . * Coordinate submission and approval of journal articles, manuscripts ... Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn… more
    Penn Medicine (11/07/25)
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  • Research Data Coordinator 1 - Medical…

    Georgetown Univerisity (Washington, DC)
    …to making a difference in the world. Requirements Job Overview The Research Data Coordinator 1 position is responsible for data management for phase I, II, and III ... oncology clinical trials...varying complexity and disease indication. + Works collaboratively with trial stakeholders and internal study teams (physicians, Regulatory team,… more
    Georgetown Univerisity (09/24/25)
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  • Research Project Coordinator (Research…

    Johns Hopkins University (Baltimore, MD)
    …**Technical Skills & Expected Level of Proficiency** + Administrative Skills - Awareness + Clinical Trial Management System - Awareness + Data Entry - Awareness ... seeking a **_Research Project Coordinator_** who will administratively coordinate research protocol implementation, typically for a single study. Will ensure the… more
    Johns Hopkins University (11/20/25)
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  • Research Project Coordinator (Research…

    Johns Hopkins University (Baltimore, MD)
    …**Technical Skills & Expected Level of Proficiency** + Administrative Skills - Awareness + Clinical Trial Management System - Awareness + Data Entry - Awareness ... We are seeking a **Research Project Coordinator ** who will administratively coordinates research protocol implementation, typically for a single study. Will… more
    Johns Hopkins University (11/05/25)
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  • Research Project Coordinator II

    Baylor Scott & White Health (Dallas, TX)
    …and external auditors and monitors. Prepares supporting documents, including the clinical protocol , investigator's brochure, case report forms, informed consent ... **JOB SUMMARY** The Research Project Coordinator II is responsible for planning, developing, implementing,...principles and practices of developing, administering and implementing a clinical trial in compliance with sponsor, federal,… more
    Baylor Scott & White Health (11/20/25)
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  • Research Assistant - Data Coordinator

    Dartmouth Health (Lebanon, NH)
    …* Primarily supports subject management, such as, performs data entry in the Clinical Trial Management System (CTMS) and supports data entry needs of ... works closely with other research staff and supports data entry for clinical trials. The Research Assistant has no supervisory responsibilities and works under… more
    Dartmouth Health (11/26/25)
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  • Data Entry Coordinator

    Actalent (Hollywood, FL)
    …with Clinical Operations, Quality, Regulatory, CROs, Sponsors, and key clinical trial personnel. + Accurately and efficiently transcribe data from ... Title: Data Entry CoordinatorJob Description Under moderate supervision, the Data Entry Coordinator I accurately transcribes clinical research data from source… more
    Actalent (11/19/25)
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  • Clinical Research Nurse- Endocrinology

    UNC Health Care (Hendersonville, NC)
    …responsible for providing and coordinating clinical care for patients enrolled in a clinical trial while adhering to all FDA, OHRP and GCP guidelines and ... data collection, data recording and follow up. Responsibilities: . Identifies potential clinical trial patients and collaborates with the physician investigator… more
    UNC Health Care (11/07/25)
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  • Senior Clinical Research Specialist…

    J&J Family of Companies (Irvine, CA)
    … trial sites (eg site management). + Contributes towards development of clinical trial documents (eg study protocol , informed consents, CRF, monitoring ... protocol compliance and data collection support to the clinical trial sites. + Contributes to the...+ Supports project/study budget activities. + May act as Clinical Safety Coordinator . + Mentors team members.… more
    J&J Family of Companies (11/26/25)
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  • Clinical Research Specialist - Mentor, Inc.

    J&J Family of Companies (Irvine, CA)
    … trial sites (eg site management). + Assists in the development of clinical trial documents (eg study protocol , informed consents, CRF, monitoring plan, ... protocol compliance and data collection support to the clinical trial sites. + Assists in tracking...in tracking assigned project budgets. + May act as Clinical Safety Coordinator . + Function as a… more
    J&J Family of Companies (11/26/25)
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