University of Kentucky
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Posting Details
Posting Details
| Job Title | Research Associate Clinical II |
|---|---|
| Requisition Number | RE43424 |
| Working Title | |
| Department Name | 40833:CCTS Clinical Research Dev & Ops Center |
| Work Location | Lexington, KY |
| Grade Level | 43 |
| Salary Range | $18.99-30.38/hour |
| Type of Position | Staff |
| Position Time Status | Full-Time |
| Required Education |
BS |
| Click here for more information about equivalencies: | https://hr.uky.edu/employment/working-uk/equivalencies |
| Required Related Experience |
3 yrs |
| Required License/Registration/Certification | CERTIFIED |
| Physical Requirements | Long periods sitting at a computer requiring strong concentration. Light lifting of 10 pounds or less. |
| Shift | Weekday Daytime, i.e. Monday – Friday, 8:00 am – 5:00 pm, |
| Job Summary | The Center for Clinical and Translational Science (CCTS) is seeking a highly motivated, professional Research Associate Clinical I to contribute to the diversity and excellence of our department and to assist the faculty and staff of our fast-paced research center. The CCTS supports campus research professionals to ensure they are able to meet their research goals and ultimately improve the health of our communities and populations. Our vision is to cultivate a diverse and inclusive environment that guides and transforms our approaches to healthcare, education, research and community partnerships. We believe that the innovation, collaboration, and rigor that result from diversity, equity, and inclusion are critical to our mission of funding innovative, early stage translational research. The CCTS’s vision is to catalyze clinical and translational discoveries through an integrated and transformative research environment targeting improved health, with emphasis on underrepresented populations in Kentucky. In support of that vision, the Research Associate Clinical I role will serve as a team member of the Regulatory Knowledge and Support Core. Responsibilities for this position are that the employee will function as a key liaison for regulatory start-up, maintenance and close-out for principal investigators and their clinical research teams and clinical research personnel in the CCTS. This position will serve as a team member of the Regulatory Knowledge and Support Core to maintain study workflow and timeline documents. Successful candidates will possess knowledge of regulatory requirements for human subject’s research. Knowledge of International Conference on Harmonization – Good Clinical Practice (ICH–GCP) and FDA regulations and procedures. Effective oral and written communication skills, exemplary organizational skills, attention to detail, multi-tasking and time management skills are a must. Must be able to work in a team and independent environment. Familiar with the use of Oncore, REDCap and UK’s eIRB system. The CCTS is committed to diversifying our staff and faculty. Individuals from diverse backgrounds are especially encouraged to apply. The University of Kentucky is proud to be an Equal Employment Opportunity (EEO). We are committed to cultivating a workplace in which diverse perspectives and experiences are welcomed and respected. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, ethnic origin, sex, age, disability (physical or mental), pregnancy, marital or veteran status, uniformed service, genetic information, sexual orientation, gender identity, gender expression, political ideology, social or economic status, whether a person is a smoker or nonsmoker as long as the person complies with University policy concerning smoking or membership in any other legally protected class. We encourage individuals with diverse backgrounds to apply. If due to a disability you need assistance/and or a reasonable accommodation during the application or recruiting process, please send a request to Eileen Zahn, [email protected], CCTS HR Manager |
| Skills / Knowledge / Abilities | Knowledge of IRB and regulatory requirements for human subject’s research, knowledge of clinical research, Microsoft Office, Oncore, REDCap familiar with Web-based reporting software. Effective oral and written communication, attention to detail, multi-tasking, time-management, organizational and interpersonal skills required. |
| Does this position have supervisory responsibilities? | No |
| Preferred Education/Experience | BS Science or health related field Master’s degree preferred |
| Deadline to Apply | 01/18/2024 |
| 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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