As a key member of the Hematology clinical research team, you will be working on four to five protocols at any given time. Your primary responsibilities will revolve around patient screening and enrollment, placing orders, and regulatory work. You will act as a liaison among key stakeholders in the institution and facilitate study team meetings. Each day will be different and flexibility is important since you will be juggling multiple studies and responsibilities. Study deadlines needs to be met while navigating the logistics of scheduling around patient visits. This job provides a great growth opportunity to learn the clinical research process from start to finish. Take the first step to join our team by applying now.
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