This position will work as part of a team in the General and Clinical Research Unit (GCRU) at the Clinical and Translational Science Institute. Will work with and assist the GCRU Registered Nurses and the Director of Clinical Research Operations with protocol specific clinical trials. Will ensure a compliant, safe and welcoming environment for the GCRU study participants, Principal Investigators and Study Coordinators. Maintain medical equipment and logs to ensure that safety standards are followed. Cover the GCRU reception desk as needed.
Bachelor's degree is helpful
1-3 years of experience working in a clinical trial/study setting is helpful
High School diploma required
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. We are a VEVRAA Federal Contractor.
Internal Number: 3234
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