Clinical Research Coordinator / Registered Nurse

    Highlights

    The Clinical Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data. Responsibilities: This position is responsible for working collaboratively with multidisciplinary teams, research and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research.

    Numbers & Facts

    LocationTopeka, Kansas

    Description

    Overview:

    Join our team as a day shift, full-time, Clinical Research Coordinator Registered Nurse in Topeka, Kansas.  Must be an Registered Nurse.

     

    Why Join Us?

     

    Thrive in a People-First Environment and Make Healthcare Better

    • Thrive: We empower our team with career growth opportunities, tuition assistance, and resources that support your wellness, education, and financial well-being.
    • People-First: We prioritize your well-being with paid time off, comprehensive health benefits, and a supportive, inclusive culture where you are valued and cared for.
    • Make Healthcare Better: We use advanced technology to support our team and enhance patient care.

    Get to Know Your Team:

    • The University of Kansas Health System St. Francis Campus, a part of a rich legacy of compassionate care since 1909, now offers 378 licensed beds, a history of innovation, and strong community support.
    Responsibilities:
    • This position is responsible for working collaboratively with multidisciplinary teams, research and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research.
    • The Clinical Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data.
    • Monitor participants’ progress including documenting and reporting adverse events. Participate in periodic quality assurance audits of protocols.
    Qualifications:

    Job Requirements:

    • Must be an RN
    • 2 Years of Clinical Research experience and a Bachelors degree required.

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