Clinical Trials Nurse Practitioner

Company: Integrated Resources, Inc
Location: Peoria
Posted on: March 19, 2023

Job Description:

Position: Clinical Trials Nurse Practitioner
Duration: 11+ Months
Location: -Peoria, AZ
Schedule: 65 hrs. in 2-week period 3 days one week, 4 days the next with every other weekend commitment
Hours: Monday-Friday 8:30am 7:30pm with 60 min lunch at 1:30pm
Saturday: 9-5:30pm with 30 min lunch at 1 pm
Sunday: 9-4:30pm with 30 min lunch at 1 pm
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Sample: Week 1: Monday/Tuesday/Friday/Saturday Week 2: Sunday/Wednesday/Thursday
Position Summary:

• 
  
• The Clinical Trials Nurse Practitioner delivers patient care services in a retail clinic environment.
  
• You will work in collaboration with a dedicated team of professionals as you independently provide holistic, evidenced-based care inclusive of accurate assessment, diagnosis, treatment, management of health problems, health counseling, and disposition planning for our patients, who are age 18 months and above.
  
• Encounters are documented utilizing an electronic health record (EHR).
  
• Clinical Trials Nurse Practitioner report directly to the Senior Practice Manager.
  Serve as a Sub-Investigator clinician for the clinical trials site, ensuring all elements of clinical trials work are completed in compliance with standard operating procedures.
  
• The Sub-Investigator is under the supervision of the Principal Investigator and is responsible for performing study related procedures and /or to make important study-related decisions in compliance with the ethical conduct of the study.
  
• Ability to perform Basic Life Support (BLS) assistance, including but not limited to performing CPR and operating an Automated External Defibrillator (AED).
  
  Primary Duties Responsibilities:
  
  
  • 
    
  • Responsibilities include but are not limited to.
    
  • Perform all study responsibilities in compliance with the IRB approved protocol.
    
  • Document all findings in subject specific source documents.
    
  • Provide ongoing assessment of the study subject/patient to identify Adverse Events
    
  • Ensure proper documentation and reporting of all Adverse Events and Serious Adverse Events
    
  • Perform physical examinations as part of screening evaluation and active study conduct.
    
  • Provide medical management of adverse events as appropriate.
    
  • Communicate with Sponsors and auditors as requested.
    
  • Possess a working knowledge of GCP/ICH guidelines, Clinic SOPs, QA/QC procedures, and Investigator 1572 Form.
    
  • Review Investigator's Brochure prior to performing any study related activities.
    
  • Participate in on-call activities as required to ensure adequate medical coverage.
    
  • Monitor safety and well-being of study participants at all times.
    
  • Educate patients on health maintenance and respond to patient care inquiries.
    
  • Document all patient care within an EHR according to company policies and procedures.
    
  • Provide care and coordination of our patients with internal and external colleagues, including the broader patient centered medical home, ensuring the highest standard of care is provided for all patients and at all times.
    
  • Effectively work within a patient care team, including fellow Providers, Collaborative Physicians, paraprofessionals, Pharmacists and other members of the health care team
    
    Responsibilities include but are not limited to:
    
    
    • 
      
    • General study coordination activities
      
    • Review participants inclusion and exclusion criteria
      
    • Collect medical history.
      
    • Physical exam
      
    • Collect vitals: body temp, pulse oximetry, respirations, heart rate*** etc.
      
    • Specimen collections and diagnostic assays
      
    • Facilitate patient surveys and questionnaires.
      
    • Patient education
      
    • Patient scheduling
      
    • Treatment administration
      
    • Liaison with the project management team the PIs clinical research team
      
    • Other activities in support of the conduct of the research protocol in accordance with all Federal, State, Local, and Client guidelines.
      
      Education:
      
      
      • 
        
      • Master's Degree level Family Nurse Practitioner program with current National Board Certification and State of Employment license to practice in the Advanced Practice Nurse role required.
        
        #hczr1

Keywords: Integrated Resources, Inc, Peoria , Clinical Trials Nurse Practitioner, Healthcare , Peoria, Arizona