• Job Description

  Req#: 46993744

  Primary City/State:

  Phoenix, Arizona

  Department Name:

  PET

  Work Shift:

  Day

  Job Category:

  Research

  Health care is constantly changing, and at Banner Health, we are at the front of that change. We are leading health care to make the experience the best it can be. We want to change the lives of those in our care and those who choose to take on this challenge. If changing health care for the better sounds like something you want to be part of, we want to hear from you.

  As a Clinical Research Coordinator in Imaging, you will be responsible for the coordination and conducting of research Imaging visits for externally sponsored projects. In addition, you will be performing image de-identification and uploads to sponsor organizations as well and scheduling, patient registrations, and compiling/submitting data related to patients engaged in applicable research studies. Every day brings a new challenge and opportunity for continued growth and development. The typical schedule for this role is M-F 8:30A-4:30P with some schedule flexibility. This is an in-person role at the Banner Alzheimer's Institute – Phoenix at 901 E. Willetta St, Phoenix, AZ 85006.

  If Clinical Research is your passion and you are looking to start your career growth, apply today and start your journey with us here at Banner Alzheimer's Institute in Phoenix, Arizona!

  Your pay and benefits (Total Rewards) are important components of your Journey at Banner Health. Banner Health offers a variety of benefit plans to help you and your family. We provide health and financial security options, so you can focus on being the best at what you do and enjoying your life.

  Banner Alzheimer's Institute (BAI) was established in 2006 as Banner Health's first Center of Excellence. Banner Sun Research Health Institute (BSHRI) was founded in 1986. Banner Health is one of the largest nonprofit health care systems in the United States. Our team is uniquely, passionately, and strategically committed to ending Alzheimer's disease and other neurodegenerative disorders without losing another generation and to providing an unparalleled model of care for families facing this devastating disease. Banner Research is committed to improving people's lives through comprehensive patient care and advances that capitalize on the best biomedical research. We intend to make a transformational difference in Alzheimer's disease and other neurodegenerative disorders research and care.

  POSITION SUMMARY
  This position is responsible for coordinating and/or implementing assigned protocols. This position includes collecting and recording medical data and history, assisting in patient assessments, and maintaining study files.
  
  CORE FUNCTIONS
  1. Provides study information and obtains relevant information to and from patients engaged in clinical studies, which includes: assisting in the recruitment and screening of volunteers; registering patients; providing information on clinical trials and protocols to interested participants in a timely and helpful manner; obtaining relevant medical history on candidates by phone and in person; collecting previous relevant medical records data on patient; explaining procedures and consent forms; compiling all information prior to the initial visit; responding to inquiries from study participants or collateral informants in a timely and helpful manner; updating databases with patient information; and/or, performing other related activities.
  
  2. Performs tasks required by protocol, which may include obtaining patient medical history, systems review, phlebotomy, EKG, and cognitive assessment on patients. Collects vital signs. Maintains quality assurance on designated protocols. Collects data as required and assists in interpreting and evaluating results as required.
  
  3. Triages adverse events and communicates with the research physician regarding the occurrence of adverse events. Collects information regarding indicated medical follow-up with the subject and collateral informants as needed.
  
  4. Provides educational information to patients and their families. Serves as a resource and support person for patients and families by being a consistent person they can contact within the clinical research program. Provides information to the patient and family related to the healthcare of the patient such as health maintenance, prevention, and anticipatory guidance relevant to study-related diseases.
  
  5. Ensures uniform implementation of protocols by completing required documentation in a consistent, accurate and timely manner. Assists in preparing appropriate IRB (Institutional Review Board) forms, informed consents, correspondence with sponsor, etc., in an accurate and timely manner. May participate in the annual IRB approval and update process.
  
  6. Serves as a liaison to other departments and programmatic areas, as well as community agencies.
  
  7. Ensures that primary referring physicians receive timely progress notes on the patient's diagnosis and treatment.
  
  8. May assume primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner.
  
  9. Department level responsibility. Some positions may have frequent interaction with patients, families, visitors, physicians, and related clinical departments.
  
  MINIMUM QUALIFICATIONS
  Must possess knowledge of clinical research methodologies as normally obtained by the completion of a Bachelors Degree in a healthcare field.
  
  Incumbents must be working towards obtaining Clinical Research Coordinator Certification (CRCC).
  
  Experience typically gained through two to four years clinical research experience. Familiarity with medical and clinical terminology. Must have excellent organizational and task management skills. Ability to maintain confidentiality of patient and study information. Ability to maintain knowledge of Federal and State regulations governing practice as well as Institute policies and procedures related to medical and nursing practice. Excellent human relations, organizational and communication skills are required.
  
  PREFERRED QUALIFICATIONS
  Possession of Clinical Research Coordinator Certification (CRCC).
  
  Additional related education and/or experience preferred.

  EOE/Female/Minority/Disability/Veterans

  Our organization supports a drug-free work environment.

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• About the company

  Banner Health is a non-profit health system in the United States, based in Phoenix, Arizona.

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