The Project Coordinator will support a wide range of educational and clinical research activities. This includes patient interviewing, obtaining informed consent, respiratory testing support, clinical data extraction from charts and entry, basic database management and statistical analyses, as well as bibliographic searches and administrative support for educational activities and for compliance purposes. Hybrid arrangements are possible, with at least 50% in-person work expected. A minimum one-year commitment is preferred.
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Job Type
Full-time
Career Level
Entry Level