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    STEPS Research Associate Clinical - Lexington, United States - InsideHigherEd

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    Description
    Job Title:

    STEPS Research Associate Clinical

    Requisition Number:

    TE08007

    Department Name:

    7H024:MCC - CLINICAL RESEARCH ORG

    Work Location:

    Lexington, KY

    Salary Range:

    $ $23.00

    Type of Position:

    Temporary

    Position Time Status :

    Full-Time

    Required Education:

    Bachelor's degree

    Required Related Experience:

    one year of experience in clinical research, data entry/management, administrative duties &/or experience in a healthcare facility

    Required License/Registration/Certification:

    NA

    Physical Requirements:

    Requires handling of light-weight objects up to 10 pounds, sitting for long periods of time, some standing or walking, repetitive motion

    Shift:

    Monday-Friday 8:00 am – 4:30 pm (40.0 hours)

    Job Summary:

    The Markey Cancer Center is currently seeking to fill a Research Associate Clinical I position to work with one of our clinical trials teams. The primary responsibilities for this position include: obtain, abstract and collate data, reports related to studies from patient medical records; maintain and submit all reports, forms and updated records to groups required by study; assist in designing a system for organizing, planning and controlling workflow related to the conduct of clinical studies and protocols; coordinate flow of patient through clinical study or protocol, monitoring all events related to patient and communicating any pertinent information to investigators and appropriate health professionals; learn basics of Good Clinical Practice (GCP) and standard operating procedures (SOP); monitor patient safety and general well-being; assist investigators with identification and recruitment of patients; ensure that pre-study and eligibility requirements of the protocol have been met for patients; maintain cooperative and professional relationships with all Clinical Research participants, other health professionals and study sponsors and/or monitors in planning care for study participation and to ensure protocol compliance; and other duties as assigned.

    This position has the potential to have a fully onsite work arrangement.

    Skills / Knowledge / Abilities:

    Planning & organization, communication (written & verbal), time management, Microsoft Office Windows, Outlook, Excel & Word; BLS certification, phlebotomy training, ECG training, EPIC, OnCore

    Does this position have supervisory responsibilities? :

    No

    Preferred Education/Experience:

    Bachelor's degree in a health related field and 1 year of experience with clinical trials; previous experience with data management, or in a health care facility preferred.

    Deadline to Apply:

    06/11/2024

    University Community of Inclusion:

    The University of Kentucky is committed to a diverse and inclusive workforce by ensuring all our students, faculty, and staff work in an environment of openness and acceptance. We strive to foster a community where people of all backgrounds, identities, and perspectives can feel secure and welcome. We also value the well-being of each of our employees and are dedicated to creating a healthy place to work, learn and live. In the interest of maintaining a safe and healthy environment for our students, employees, patients and visitors the University of Kentucky is a Tobacco & Drug Free campus.

    As an Equal Opportunity Employer, we strongly encourage veterans, individuals with disabilities, women, and all minorities to consider our employment opportunities.

    Any candidate offered a position may be required to pass pre-employment screenings as mandated by University of Kentucky Human Resources. These screenings may include a national background check and/or drug screen.



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