Primary City/State:
Sun City, Arizona
Department Name:
Neuropath-Lab Overhead-Rsrch
Work Shift:
Day
Job Category:
Research
Find your path in health care. We want to change the lives of those in our care – and the people who choose to take on this challenge. If you’re ready to change lives, we want to hear from you.
At Banner Research, the Brain and Body Donation Program needs a Clinical Research Assistant. This department offers a unique team environment. You will be involved in scheduling and interacting with research visits and participants. In addition, you will be participating in study related visit activities and completing administrative tasks associated with research projects.
Your pay and benefits are important components of your journey at Banner Health. Banner Health offers a variety of benefits 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 Research is at the leading edge in a new era of scientific discovery and innovation. Our basic and clinical research faculty turns ground-breaking research findings into new identification, treatment and prevention methods for diseases such as Alzheimer's, Parkinson's, Cardiovascular disease, Cancer and Orthopedics. We have an international reputation for our work and we provide outstanding access for patients to clinical trials. Our commitment to excellence allow us to make a difference in people's lives every day.
POSITION SUMMARY
This position is responsible for performing patient registrations, as well as compiling and submitting data related to patients engaged in applicable research studies. Monitors study compliance and maintains a system for effective data flow associated with research protocols.
CORE FUNCTIONS
1. Maintains current and accurate protocol documentation and notifies appropriate individuals of pertinent protocol changes. Identifies and communicates important protocol and data management issues to appropriate individuals.
2. Verifies that patients have completed appropriate registration materials and maintains related records and information.
3. Instructs volunteers on protocol requirements and explains procedures and consent forms. Ensures related documentation is properly completed.
4. Ensures protocol compliance with intense monitoring of specific study requirements and schedules protocol related treatment and tests. Performs specific clinical duties as required per the research study.
5. Assists in ordering and maintaining research supplies as directed.
6. Prepares and maintains a variety of documentation in assigned area of responsibility.
7. May serve as a backup, collecting and delivering specimens for analysis using appropriate or specified equipment. Ensures proper labeling and obtains pertinent clinical and protocol information on request forms.
8. Department level responsibility. Some positions may have frequent interaction with patients, families, visitors, physicians, and related clinical departments.
MINIMUM QUALIFICATIONS
High school diploma/GED or equivalent working knowledge.
Knowledge of basic laboratory procedures as normally obtained through the completion of two years experience in a health care setting, preferably in a research environment. Must have knowledge and understanding of medical terminology in order to read, identify, and extract pertinent data from medical records and information. Must be able to multi-task and re-prioritize duties as needed. Ability to maintain confidentiality. Excellent human relations, organizational and communication skills are required.
Must be knowledgeable of data entry and computer programs associated with maintaining databases, spreadsheets, etc.
PREFERRED QUALIFICATIONS
Associate’s Degree or Certified Research Assistant Certification preferred.
Additional related education and/or experience preferred.
