Nationwide Children's Hospital

  • Clinical Research Coordinator RN- Direct Patient Care- Cellular Therapy

    Posted Date 1 month ago(6/8/2018 1:53 PM)
    Requisition ID
    2018-12056
    Category
    Nursing
  • Overview

    Come work for an organization where everything matters.


    Full-time position, working 40 hours per week, Day shift hours from 8am-4:30pm, EXEMPT position, Benefits eligible.

     

    Looking for experienced BMT nurse with interest in clinical research.

    Starting minimum payrate: $25.676/hr

     

    The Clinical Research Coordinator RN’s primary responsibility is the overall administrative coordination and management of patients while receiving research treatment in the area of Cellular Therapy.  These responsibilities include but are not limited to: implementation of protocol at time of startup, therapy order sets, patient compliance, source documentation, data collection, specimen processing, and day to day management of study participants. 

    Responsibilities

     

    The Clinical Research Nurse (CRN) prescribes, delegates, supervises and provides patient care, plans for education, collaborates on care plans and provides for patient safety and quality while the patient is involved in the clinical research trial. In addition, the CRN performs all research activities and procedures as outlined in the protocol; implementing and organizing each clinical research trial they are assigned to, to ensure all federal, state and institutional compliance are followed as well as implementing the trial in the most beneficial way for the patient and their family.

    Demonstrates nursing competencies to provide age-appropriate care to patients from the age of birth through 21 years, and select adult patients while maintaining the integrity of each clinical trial protocol and patient safety while enrolled in a clinical trial.

    Responsibilities:

    1. Creates clinical trial source documents to ensure all elements of clinical trial protocol are captured at protocol required time points; comparing source documents created to protocol, informed consent document and sponsor provided case report forms or database to ensure accuracy and completeness.
    2. Provides input into the feasibility of a clinical trial; barriers to subject recruitment and budgetary needs to ensure a successful clinical trial. Attends institutional required feasibility meetings and sponsor required site assessment and study initiation visits. May also travel to sponsor required study protocol meetings.
    3. Uses nursing process, evidence based practice and unit specific competencies to:
      1. Identify those patients who meet clinical trial eligibility criteria; ensuring all inclusion criteria are met and no exclusion criteria are present by thorough medical record review, back-up documentation from outside service providers and other means necessary to ensure eligibility
      2. Conducts informed consent discussion with patient and family outlining study purpose, risks and potential benefits as well as a thorough discussion of all trial required procedures and visits; answers questions related to study participation as applicable; acts as a patient/family advocate
      3. Responsible for scheduling, completing procedures and collecting data associated with all protocol required visits in the inpatient, outpatient and community setting.

     

    1. Documents a plan of care including patient outcome parameters throughout clinical trial participation including but not limited to:
      1. Works with study physician and other ancillary service providers to ensure all protocol required procedures are done on time, exactly as indicated in clinical trial protocol and that all data components are captured to ensure compliance with protocol and regulations
      2. Evaluates patient care and patient’s response/progress; collect and document all adverse event information throughout trial participation and report to sponsor and Institutional Review Board as required
      3. Reassesses patients and revise plan of care as appropriate; collaborates with study physician to determine when a patient should be withdrawn from a clinical trial due to non-compliance or safety concerns
      4. Supervises patient care and safety throughout clinical trial participation
      5. Plan, provide, delegate, and evaluate patient/family education related to the study medication and clinical trial.

     

    1. Collaborates effectively and communicates patient care needs/expectations/priorities related to clinical trial participation to all involved care providers including unit nursing staff, attending physician, ancillary service providers (radiology, cardiology, physical therapy, pharmacy, etc.) to facilitate positive patient outcomes both in clinical care and in clinical trial participation.

     

    1. Completes all protocol required procedures including but not limited to venipuncture, IV start, medication administration, EKG’s and all other nursing procedures and assessments.

     

    1. Prepares and processes human specimens for use in research studies. Collects blood, urine, and other samples as required by protocol. Performs CLIA waived laboratory assessments. Obtain and maintain IATA certificate.

     

    1. Responsible for managing all data elements associated with clinical trial implementation, execution and close out. Ensures all data elements are collected at protocol required time points; lab, diagnostic reports requiring medical interpretation are reviewed and signed off by an investigator in accordance with all applicable regulations; documentation about clinical trial participation is maintained in each subjects research record in an organized way; completes Case Report Forms (CRFs) prior to monitor visits as instructed by the sponsor; archives all clinical trial related documentation once study close out visit has occurred.

     

    1. Works with study physician to provide and document initial clinical trial training for all study team members and ancillary service providers; initiates and maintains documentation for all subsequent protocol required training due to amendments, risk changes, visit procedure changes etc.  

     

    1. Responsible for management of regulatory/IRB issues after a clinical trial has been initiated; maintains regulatory binder in conjunction with the regulatory coordinator office.

     

    1. Schedules, prepares study data for, and attends monitor visits, audits, or other meetings as required for the study. Works with Research Compliance when audited by sponsor, FDA, DEA or other governmental agency; attends audit meetings and works with regulatory, compliance and study team to respond to audit findings.

     

    1. Participates in and adheres to departmental quality improvement initiatives to maximize quality data collection and compliant study conduct; peer review QA of all consent and inclusion/exclusion visit documentation; protocol implementation checklist; monthly study metric reporting; provides input into unit policy development and revisions and Standard Operating Procedures (SOP).

     

    1. Participates in unit maintenance activities as well as Patient Care Services and Hospital activities:
      Safety Huddles within 24 hours of a safety event; Zero Hero initiatives
      b. Infection control activities
      c. Joint Commission readiness

     

    1. Participates in educational activities in one or more of the following:
      Peer review
      b. Serves as a preceptor/clinical research resource
      c. Orientation and continuing education
      d. Clinical research competency development and assessment
      e. Planning and presenting classes and presentations internally and at national conferences.

     

    1. Adheres to unit/department budgetary standards; keeps weekly time sheet and enters time into eTrac to ensure projects are charged for time spent and unit maintains adequate chargeback ratio to meet annual operating budget

     

    1. Practices professional nursing in accordance with the ANA Code of Ethics for Nurses.

     

    Maintains flexible schedule daily based on study/unit needs; working days, evenings, weekends, longer shifts and overnight as well as on call, as dictated by protocol requirements to ensure visits, procedures and data are collected at protocol required time points so that each clinical trial is in compliance with all appropriate regulations.

    Qualifications

    MINIMUM QUALIFICATIONS: 

     

    1. Licensure: Licensed as a Registered Nurse in the State of Ohio.
    2. BSN; Associate degree with commitment to obtain BSN within 5 years of hire.
    3. Current CPR certification. Must be willing to obtain and maintain NRP and PALS certification as determined by your manager.
    4. Demonstrates proficiency in clinical nursing skills such as venipuncture, IV starts and injections
    5. Understanding of medical terminology and clinical trials preferred.
    6. Skills required:
    • Working knowledge of PCs, word processing, and data management software
    • Strong verbal, written, interpersonal communication
    • Goal-oriented; self-directive
    • Initiation, self-motivation, creativity, flexibility
    • Organizational and detail oriented
    • Ability to actively participate as a team player

    Note frequency as Constantly (67-100%), Frequently (34-66%) and Occasionally (0-33%) for each requirement.  Also note any lifting requirements with pound limit.

     

     

    MINIMUM PHYSICAL REQUIREMENTS:

     

    Talking on phone/in person; frequently (34-100%)

    Sitting; frequently (34-100%)

    Standing/Walking; frequently (34-100%)

    Lifts objects weighing up to 25 pounds; occasionally (0-33%)

    Typing on keyboard; occasionally (0-33%)

     

    Columbus

     

    EOE M/F/Disability/Vet

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