CLINICAL RESEARCH NURSE COORDINATOR I

University of Alabama at Birmingham, United States

Updated: 3 months ago
Location: Birmingham, ALABAMA

CLINICAL RESEARCH NURSE COORDINATOR I - (T213928)

Description

 

The Clinical Research Nurse Coordinator I position will be a part of the Transplant Clinical Research team for kidney transplantation. Assigned studies will range from registry studies to intervention studies involving post-transplant patients.

General Responsibilities

  • To serve as coordinator for clinical research studies and provides support to other study team members for research trials, studies, and projects within the confines of the study protocols as directed.
  • To support protocol screening and study participant eligibility determination, working with more senior study team members to ensure compliance.
  • To conduct all study activities in accordance with the protocol, Institutional Review Board (IRB) regulations, and Good Clinical Practice (GCP). May provide quality care to participants and their families within the area of clinical specialty.
  • To assist with the life cycle of the study from start-up through maintenance to closure.
  • To coordinate and organize participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
  • To perform the informed consent process following GCP.
  • To act as a liaison among the clinical and research staff, departments, ancillary services and the study sponsor to ensure protocol compliance throughout the study.

Key Duties & Responsibilities

  • Responsible for the collection of clinical research data, recording, and maintaining data.
  • Develops and maintains databases.
  • Ensures accuracy of documentation.
  • Acts as liaison with sponsor, CRA, Research Pharmacy, IRB, OSP, and enters all required data into OnCore and sponsor CRFs.
  • Coordinates and conducts patient care visits and assure all procedures are conducted in compliance with the protocol.
  • Schedules tests and procedures.
  • Interacts with the PI to assure the patient receives appropriate medical evaluation and care when needed and will alert PI of any serious adverse events that may occur throughout the course of the study.
  • Reports all adverse events to the sponsor and all serious adverse events to the IRB and sponsor.
  • Recruits, screens, enrolls, and schedules participants for appropriate research projects.
  • Collaborates with Principle Investigators (PI), sponsors, and research team in the evaluation and coordination of protocols, budgets, recruitment strategies, and data management plans.
  • Identifies potential and/or inconsistencies.
  • Performs other duties as assigned.

    • Annual Salary Range:      $52,555 - $68,320

     

    Qualifications

     

    Bachelor's degree in a related field required. Work experience may substitute for education requirement. Currently licensed or eligible to be licensed as a Registered Nurse (RN) by the Alabama Board of Nursing required.

    Preferences

    Previous research experience is preferred.

     
    Primary Location
    : University
    Job Category
    : Clinical Research
    Organization
    : 311402600 Med - Nephrology
    Employee Status
    : Regular
    Shift: Day/1st Shift
    Work Arrangement (final schedule to be determined by the department/hiring manager): Hybrid Eligible

    Similar Positions