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University of Kentucky
Lexington, Kentucky, United States
(on-site)
Posted
21 hours ago
University of Kentucky
Lexington, Kentucky, United States
(on-site)
Job Function
Other
Clinical Research Coordinator II
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Clinical Research Coordinator II
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Description
University of Kentucky
Equal Employment Opportunity/M/F/disability/protected veteran status.
Posting Details Posting Details Job TitleClinical Research Coordinator IIRequisition NumberRE52477Working TitleCRC II (PMC)Department Name7H024:MCC - CLINICAL RESEARCH ORGWork LocationLexington, KYGrade Level46Salary Range$25.01-41.25/hourType of PositionStaffPosition Time Status Full-TimeRequired EducationBSClick here for more information about equivalencies:https://hr.uky.edu/employment/working-uk/equivalenciesRequired Related Experience3 yrsRequired License/Registration/CertificationNonePhysical RequirementsRequires handling of light-weight objects up to 10 pounds, sitting for long periods of time, some standing or walking, repetitive motion.ShiftMonday-Friday 8:00am-4:30pm (40 hrs/wk)Job SummaryThe Markey Cancer Center is recruiting a Clinical Research Coordinator II to work with our Precision Medicine Clinic. The primary responsibilities for this position include: obtain, abstract and collate data, reports, etc. related to studies; 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 PI and appropriate health professionals; learn basics of Good Clinical Practice (GCP) and standard operating procedures (SOP); monitor safety and general well-being of all patients by exercising independent clinical judgment regarding patient care issues and protocol adherence; assist investigators with identification and recruitment of patients; ensure that per-study and eligibility requirements of the protocol have been met for patients, maintain cooperative and professional relationships with all Clinical Research participants; collaborate and consult with other health professional in planning care for study participation and to ensure protocol compliance; and other duties as assigned.
This position will have a fully on-site work arrangement.
IMPORTANT: Resumes and CVs cannot be substituted for a completed application. Incomplete applications could disqualify you from being considered for this position. If the information on your resume is not entered on the application, this will prevent us from being able to assess your education and experience when trying to determine a salary offer. To be considered you must fully complete the online application being sure to only put one (1) job title for each entry (multiple job titles for one employer must have separate entries), the # of hours worked per week and your ending salary. You will also be required to upload a cover letter and resume.
To view our exceptional benefits, please visit https://www.uky.edu/hr/benefits.
Skills / Knowledge / AbilitiesStrong attention to detail and excellent organizational skills. Proficient in operating various office machines including computers, printers, and various software packages. Robust interpersonal skills. Advanced knowledge of Microsoft Office products. Strong written and verbal communication skills. Initiative, collaboration, advanced time management skills. Technical skills applicable to essential functions and initiative.Does this position have supervisory responsibilities? NoPreferred Education/ExperienceBachelors degree + 3 years experience. UK equivalencies apply. Certification preferred (CCRC, CCRA, CCRP, etc.)Deadline to Apply12/09/2025Our University CommunityWe 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.
The University follows both the federal and state Constitutions as well as all applicable federal and state laws on nondiscrimination. The University provides equal opportunities for qualified persons in all aspects of institutional operations and does not discriminate on the basis of race, color, national origin, ethnic origin, religion, creed, age, physical or mental disability, veteran status, uniformed service, political belief, sex, sexual orientation, gender identity, gender expression, pregnancy, marital status, genetic information or social or economic status.
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.
Posting Specific Questions
Required fields are indicated with an asterisk (*).
- * Please select the answer that best describes your years of paid, full-time experience in clinical research.
- none
- more than 0, up through 1 year
- more than 1 year, up through 3 years
- more than 3 years, up through 5 years
- more than 5 years
- * How many years experience do you have working with protocol submissions, IRB's, patient consents?
- None
- More than 0, up through 1 year
- More than 1 year, up through 3 years
- More than 3 years, up through 5 years
- More than 5 years
- * Describe your experience working with clinical research - data management, study/coordination, patient care, patient recruitment and enrollment.
(Open Ended Question)
- * Please select the response that best represents your amount of paid, full-time employment experience working with clinical research studies and/or administering or monitoring research protocols.
- None
- More than 0, up through 1 year
- More than 1 year, up through 2 years
- More than 2 years, up through 3 years
- More than 3 years
Applicant Documents
Required Documents
- Resume
- Cover Letter
PI280313712
Job ID: 81486788
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