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Details
Posted: 10-Jan-25
Location: Lexington, Kentucky
Categories:
Healthcare
Staff/Administrative
Internal Number: 566265
Department Name: 7H030:SANDERS-BROWN CTR ON AGING
Job Summary:
The Clinical Trial Coordinator will provide critical research management to aging and cognitive impairment research projects including NIH grants.
The Clinical Trial Coordinator will be responsible for managing research participants and field data collection including storage of audits, surveys, and qualitative interviews.
This position will also assist the PI with producing reports, researching products and managing IRB submissions. Additionally, this position will have opportunities to contribute to manuscripts/presentations.
In this position, the Clinical Trial Coordinator will engage with community partners and health promotion events. Position requires on campus and community-based work time, and personal transportation is preferred.
The Clinical Trial Coordinator will be responsible for managing research participants and field data collection including storage of audits, surveys, and qualitative interviews.
This position will also assist the PI with producing reports, researching products and managing IRB submissions. Additionally, this position will have opportunities to contribute to manuscripts/presentations.
In this position, the Clinical Trial Coordinator will engage with community partners and health promotion events. Position requires on campus and community-based work time, and personal transportation is preferred.
Skills /Knowledge/Abilities:
Advanced leadership skills and empathy. Extensive knowledge and experience with the implementation of study-related activities. Excellent verbal and written communication skills. High-level organizational skills. Able to problem-solve independently and collaboratively.
Position Time Status: Full-Time
Required Education:
BS
Required Related Experience:
5 yrs
Required License/Registration/Certification :
None
Preferred Education/Experience:
Bachelor's degree and at least 5 years of research experience. Clinical research certification (CCRC, CCRA, CCRP, etc.) preferred.
University Community of Inclusion:
We value the well-being of each of our employees and are dedicated to creating a healthy place for everyone 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.
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.
About University of Kentucky
Adjacent to downtown Lexington, UK is nestled in the scenic heart of the beautiful Bluegrass Region of Kentucky. UK's campus covers more than 814 acres, with more than 30,700 students and 13,500 full-time employees, including nearly 2,400 full-time faculty and librarians.
More Jobs from This Employer
https://main.hercjobs.org/jobs/20965190/clinical-research-coordinator-iii
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