The Data Coordinator collects, enters or transcribes, and transmits or submits clinical data for assigned investigational drug studies. The role handles paper and electronic case report forms (CRFs), including corrections and query resolution, and helps ensure assigned study data is complete, accurate, and current. The coordinator receives and requests patient records from the study team, reviews protocols as guides for study activities, and coordinates monitor visits and related meetings. The position is based at START in Pittsburgh and works Monday through Friday, 8:00 a.m. to 5:00 p.m.
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Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED