• Clinical Research Assistant Senior

    Job Number
    North Colorado Medical Ctr
    WR Admin-Region-SS
    Address : Street
    1801 North 16th St
    Address : Location
    Work Schedule
    Position Type
    FT: Full-Time
    Posting Category
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    About Banner Health - Western Region
    Whether you are seeking a clinical or non-clinical career, you will have the opportunity to apply your unique experience and expertise in support of a nationally-recognized healthcare leader. Banner Health's Western Region consists of facilities that offer comprehensive care in friendly, small-town environments. With Banner Health Western Region you get a unique combination of the latest technology at your workplace and relaxed living.



    About Banner Health
    Banner Health is one of the largest, nonprofit health care systems in the country and the leading nonprofit provider of hospital services in all the communities we serve. Throughout our network of hospitals, primary care health centers, research centers, labs, physician practices and more, our skilled and compassionate professionals use the latest technology to make health care easier, so life can be better. The many locations, career opportunities, and benefits offered at Banner Health help to make the Banner Journey unique and fulfilling for every employee.


    Job 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.


    Essential Functions

    • 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.


    • Verifies that patients have completed appropriate registration materials and maintains related records and information.


    • Instructs volunteers on protocol requirements and explains procedures and consent forms. Ensures related documentation is properly completed.


    • 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.


    • Assists in ordering and maintaining research supplies as directed.


    • Prepares and maintains a variety of documentation in assigned area of responsibility.


    • 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.



    Minimum Qualifications

    High school diploma/GED or equivalent working knowledge.

    Experience typically gained through two to four years clinical research experience. 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 Degree or Certified Research Assistant Certification preferred.

    Additional related education and/or experience preferred.

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