Yale New Haven Health System

  • CLINICAL RESEARCH COORDINATOR

    Job Locations US-CT-Bridgeport
    Job ID
    64700
    Department
    DEPT OF SURGERY
    Category
    RN/NURSING - ALL OTHER
    Position Type
    Part Time Benefits Eligible
    Scheduled Hours
    24
    Work Schedule
    DAYS
    Work Days
    MON,WED,FRIDAY
    Work Hours
    7:30-4PM
    Work Shift
    NONE
    Requisition ID
    2018-17866
  • Overview

    To be part of our organization, every employee should understand and share in the YNHHS Vision, support our Mission, and live our Values. These values—integrity, patient-centered, respect, accountability, and compassion—must guide what we do, as individuals and professionals, every day.

    At Bridgeport Hospital, we are committed to providing quality medical care and treatment that is coordinated and centered on the patient’s specific needs. We strive to achieve benchmarks as a Patient Centered Medical Home and provide health care in a setting where patients are at the center of their care team. All employees of Bridgeport Hospital are part of the patients care team and contribute to the team approach of promoting access, continuous, comprehensive care and work to provide quality improvement in the care provided to their patients.

    The Clinical Research Coordinator is responsible for the organization, management, coordination and supervision of all assigned research protocols under the direction of The Section of Trauma, Burns and Surgical Critical care. The CRC will develop, implement and coordinate research and administrative duties requiring analysis, sound judgment and a high level of knowledge of study protocols.

    EEO/AA/Disability/Veteran

    Responsibilities

    • 1. Complies with GCP's (Good Clinical Practice) guidelines and follows all FDA regulations with regard to clinical trials.
    • 2. Coordinates initiation of new research studies
    • 3. Participates in Investigators Meetings for assigned study as mandated by protocol.
    • 4. Compiles materials necessary for initiation of study protocol for presentation to staff as indicated by protocol guidelines.
    • 5. Conducts necessary in-services to Surgery and nursing staff as indicated by unit based inservice documentation sheets.
    • 6. Recruit and screen patients using protocol inclusion/exclusion criteria and enroll patients eligible into assigned study
    • 7. Conducts interviews with physicians to encourage patient recruitment as needed for study enrollment
    • 8. Ensure that the consent process has taken place effectively and all questions are answered satisfactorily and documented
    • 9. Collects study protocol data (Informed consent and required IRC outline) as required by each study for presentation to IRC as indicated by review of IRC minutes.
    • 10. Submits data, resolves and submits queries as required by study within timeframe required by study
    • 11. Advises principal investigator of progress of data collected on a monthly basis
    • 12. Responsible for processing of contract in conjunction with Bridgeport Hospital legal counsel, Sponsor, and Principal Investigator

    Qualifications

    EDUCATION

     

    Registered nurse with a current license in the State of Connecticut. BSN preferred.

     

    EXPERIENCE

     

    Minimum of three (3) to five (5) years experience of clinical nursing experience in an acute care surgical setting.

     

    LICENSURE

     

    Licensed RN State of CT

     

    SPECIAL SKILLS

     

    Excellent communication, negotiation and organizational skills. Excellent clinical judgment. Excellent knowledge of personal computers and related presentation software. Adaptability to a wide variety of processional interactions.

     

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