The position will involve study coordination for research trials within the Neuroradiology Clinical Research Division. Primary responsibilities include screening, recruitment, consenting of participants, and other research activities for both NIH and Industry-sponsored studies. Additional responsibilities include organizing and maintaining study documentation, database entry, resolving data queries, review of medical records, scheduling study-related tests in EPIC/Pennchart, Radiology, and other research systems; preparing and processing regulatory documents for submission to the IRB, and all regulatory committees from study start-up to completion. Interact with study sponsors, preparing and participating in study initiation visits, study audits, monitoring and closeout visits.
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Job Type
Full-time
Career Level
Mid Level