ResponsibilitiesThe Study Coordinator will need to be familiar with all aspects of animal and human subject regulatory work (ARC submissions, IRB submissions, tracking of adverse events, FDA regulations, DSMB coordination). Must have at least 5 years of experience in a study coordinator role for preclinical imaging and clinical research. In this role, you will also be responsible for human subject recruitment, screening, enrollment, and retention and will be expected to organize and analyze data, generate summary figures and tables, contribute to presentations and manuscript preparation. Perform various image (MRI, cardiac ultrasound or echo) post-processing and measurements as determined by t
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