Support the Clinical & Regulatory Operations team, assisting with site communications, data compliance activity, screening review efficiency and site submission efficiency.
Attend clinical cases, supporting the heart team with device prep and loading of the DurAVR valve in each assigned case.
Provision of education and guidance to physicians and site staff in identifying appropriate study patients and assist site in ensuring complete patient screening and enrollment information.
Track all patient pathway screening process activity, routinely providing metrics per site on screening and progress of enrollment.
Assist customers with inventory management, including ordering, shelf stock and ordering.
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