• Clinical Nurse Coordinator

    Posted Date 3 weeks ago(4/6/2018 10:29 AM)
    Requisition ID
    2018-42152
    Category
    Research
    Position Type
    Regular Full-Time
    Department
    TRI Clinical Research Coordinators
    Post End Date
    5/7/2018
  • Overview

    The Research Nurse Coordinator position supports the Translational Research Institute’s (TRI) Project Support Unit in its mission to provide quality, efficient, and investigator-friendly services to UAMS investigators. The position is responsible for independently coordinating research activities and performing a full range of tasks for assigned research projects/programs that include both clinical and community based research. This person works independently in the performance of routine research duties with the guidance of the Director of Clinical Trials, TRI Administration, and Investigator. This position will utilize the nursing process of assessment, planning, implementation, and evaluation to provide study related procedures to research participants in accordance with Good Clinical Practice Guidelines and human subject protection. This position practices within the limits of the Nurse Practice Act of the State of Arkansas as well as complies with UAMS policies, procedures and standards of care. This position is governed by state and federal laws and agency/institution policy. This position may require to be on-call for pre-determined dates.  

     

    UAMS offers amazing benefits and perks:

    • Health: Medical, Dental and Vision plans available for staff and family
    • Holiday, Vacation and Sick Leave
    • Education discount for staff and dependents (undergraduate only)
    • Retirement: Up to 10% matched contribution from UAMS
    • Basic Life Insurance up to $50,000
    • Career Training and Educational Opportunities
    • Merchant Discounts
    • Concierge prescription delivery on the main campus when using UAMS pharmacy

    Responsibilities

    (40%) - Coordinates and performs a range of duties in conducting research and will be actively involved in several projects and studies from several different investigators at any time. Obtains informed consent following federal, state and local regulations. In coordination with the investigator and other staff, conducts subject visits and performs study-related procedures as detailed in the protocol while ensuring the safety of the study participant as well as maintaining confidentiality of personal health information. Performs IV therapy, study drug administration, phlebotomy, process samples for shipping, and any other procedures specific to a study protocol. Reports adverse events.

                                   

    (30%) - Provides support services for assigned research projects, including development of source documents and other study related materials, completion of case report forms, electronic data entry, and participates in recruitment efforts for current studies. Prepares for study implementation by entering study information into electronic management research system(s) and creates the study in the electronic medical record system, as applicable. Accurately and completely documents all research related activities in a timely manner utilizing a variety of mechanisms both electronic and hard copy. Assists in the development of departmental research budgets in the Clinical Research Administration (CLARA) system.

     

    (20%) - Attends or facilitates meetings and other communications with investigators, research sponsors, other research staff and investigator staff members for the purposes of coordination of services to support assigned research projects. Interacts with investigators, coordinators and other healthcare providers to ensure coordination of research activities for the research participant and may provide training and/or mentoring on the conduct of research to the larger UAMS research community.  Some travel required to attend training sessions for research projects. 

     

    (5%) - Completes required training per institutional policy including but not limited to Human Subjects Protection, Good Clinical Practice, and HIPAA for Research Subjects, and International Air Transport Association (IATA) Training. Coordinate and attend implementation, investigator and other study meetings. Backs up other staff members as needed.

     

    (5%) - Other related duties as required or assigned.

    Qualifications

    Current Arkansas RN license plus 2 years of RN or Research experience required. Must have a Basic Life Support (BLS) certification or eligible to apply. Must be in good standing by the AR State Board of Nursing.

     

    Salary: Negotiable

     

    UAMS is an inclusive Affirmative Action and Equal Opportunity Employer of individuals with disabilities and protected veterans and is committed to excellence. 

    Physical Requirements

    Stand: Occasionally
    Sit: Frequently
    Walk: Frequently
    Bend, crawl, crouch, kneel, stoop, or reach overhead: Occasionally
    Lift, push, pull, carry weight: 10 lbs or less
    Use hands to touch, handle, or feel: Frequently
    Talk: Frequently
    Hear: Continuously
    Taste or smell: Occasionally
    Read, concentrate, think analytically: Continuously
    Physical Environment: Inside Medical Facility Environment, Inside Office Environment
    Noise Level: Moderate
    Visual Requirements: Far visual acuity, Near visual acuity
    Hazards: Sharp objects/tools

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