As a Senior Clinical Research Monitor, you will monitor the protocols and ensure regulatory compliance of clinical research studies with moderate to high risk research designs. These studies are conducted across numerous departments in multiple treatment areas. Responsibilities include the following:
You are expected to independently initiate and manage special projects and audits as needed as a member of the Clinical Trials Operations office. In this role, you will oversee study team members in accordance with the specific protocol documents and federal regulations. This job gives you an opportunity to work in an oncology-related role without extensive travel. Take the first step to join our team by applying now!
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