The Paley Institute
The Clinical Research Coordinator will conduct all aspects of the clinical trial, including regulatory tasks, under the direct supervision of the Physician. The Clinical Research Coodinator provides operational and administrative support in the management of patients accrued to multiple research protocols to assure subject’s safety and regulatory compliance. The Clinical Research Coodinator is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, and all applicable regulations and guidelines and ensuring effective data flow associated with research protocols.
The following experience is highly preferred:
-Experience with FDA trials, whether pharmaceuticals or devices but would love IDE trials
-Experience with billing/contracts/budgets for projects
-Interaction with study sponsors including industry and FDA
-Face to face interactions with patients whether for recruitment or followup
-Experience with GCP (Good Clinical Practice); CTMS
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