Clinical Research Coordinator: Lead Multisite Trials
SMARTFOX
SMARTFOX invites a Clinical Research Coordinator to support Phase I–IV trials across multiple therapeutic areas in the United States. You will screen and recruit participants, obtain informed consent, and coordinate study visits with data collection and regulatory compliance. Responsibilities include data entry in Medidata Rave and other EDC platforms, maintaining trial binders, IRB submissions, and AE reporting. Requires a bachelor’s degree and US work authorization. #J-18808-Ljbffr SMARTFOX
Vacancy posted 3 days ago
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