Responsibilities
The Community Practice Senior Clinical Research Associate will be responsible for ensuring protocol procedures are completed accurately, safely, and in a timely manner, this includes responsibility for research assessment and patient intervention under the supervision of the Principal Investigator. Additional responsibilities include regulatory compliance, patient recruitment and enrollment, data collection, research chart documentation, quality assurance, report preparation, protocol information dissemination to health care professionals, patients and their family members. Responsible for feasibility review of upcoming, assigned protocols with regards to study execution. Ensure investigational product is adequately managed and documented.
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