Clinical Research Associate Senior

Data Management Analyst SeniorJob Title - Data Management Analyst SeniorWorking Title - Clinical Research Associate SeniorDepartment Name - Clinical Research Support OfficeWork Location - Lexington, KYGrade Level - 44Salary Range - $44,678-71,469/yearType of Position - StaffPosition Time Status - Full-TimeRequired Education - BARequired Related Experience - 3 yrsRequired License/Registration/Certification - NonePhysical Requirements - Ability to sit for long periods of time utilizing mouse, keyboard, computer and telephone. Ability to lift, push, or pull objects up to 50 lbs.Shift - Monday – Friday, 8:00am to 5:00pm with occasional early or late meetings required.Job Summary - Shape the Future of Clinical Research Administration at the University of Kentucky Wildcat Wisdom, Kentucky Innovation – Supporting Discoveries, Transforming Outcomes! Why Join Us? The University of Kentucky's Clinical Research Support Office (CRSO) is seeking a dedicated and skilled Data Management Analyst Senior (Clinical Research Associate Senior). This vital role supports and enables groundbreaking clinical research across the University.About the Role: This position is eligible to be fully remote. Responsibilities include, but are not limited to … assisting all clinical research teams with the CRSO services including the development of the electronic schedule of events and initial data entry content reviewing and interpreting complex clinical research protocols and determines the level of data entry in the CTMS (clinical trial management system) producing clinical research calendars, to drive participant tracking, compliant billing, and financial practices in the CTMS and the proper billing charge in Epic supporting the CRSO by being the first contact with all new studies requiring CRSO services, serving as a subject matter expert for the content of each study entered into the CTMS including the minimum data requirements based on the study type, and assisting with the tracking of Epic reports related to new patients, new studies, first tier dashboard and others Collaboration with clinical research team members and other UK internal partners, in addition to possessing the ability to prioritize and manage project workload, is important to this position.The University of Kentucky uses equivalencies in determining if a potential applicant meets the minimum education and experience. Related experience can be substituted for education. Click here for more information about equivalencies: / Knowledge / Abilities - Proficient in Microsoft Office products.Does this position have supervisory responsibilities? - NoPreferred Education/Experience - Preferred experience with clinical research, clinical trial management systems, billing for clinical research, regulatory and financial administration. Research certification preferred completion within 3 years of hire date.Deadline to Apply - 11/05/2026Our University Community - 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. 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.Required fields are indicated with an asterisk (*).* Describe your experience working with clinical research, provide details and one related example. (Open Ended Question)Required DocumentsResumeOptional DocumentsCover Letter