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Clinical Research Coordinator I, II & III. STRIVE (Baton Rouge - Part Time)
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Part-time
- Summary The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials related to maternal health and diabetes.
- The Clinical Research Coordinator assists the investigator team to develop study protocols and manuals of procedures.
- The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and entry, performs noninvasive cardiovascular tests according to study protocols, and conducts small group coaching sessions.
- The Clinical Research Coordinator is also responsible for keeping all data and source documentation, adverse event reporting, and IRB regulatory files.
- Tulane offers a variety of options to enhance your health and well-being so that you may enjoy more out of life now and in the future.
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