Posted in Other 29 days ago.
Location: Lexington, Kentucky
| Job Title | STEPS Research Associate Clinical |
|---|---|
| Requisition Number | TE08007 |
| Department Name | 7H024:MCC - CLINICAL RESEARCH ORG |
| Work Location | Lexington, KY |
| Salary Range | $17.24 - $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 - 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 check and/or drug screen. |
Required fields are indicated with an asterisk (*).
PI238781788
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