Responsible for management of the clinical monitoring process and administration of clinical trials. Supervises CRAs in their function of in-house and on-site monitoring, filing, and administration of clinical trials. Oversees assurance of adherence to SOPs, Good Clinical Practice and FDA regulations. Requires a master's degree/Ph.D and at least 5 years of experience in the field or in a related area. Familiar with a variety of the field's concepts, practices, and procedures. Relies on extensive experience and judgment to plan and accomplish goals. Performs a variety of tasks. Leads and directs the work of others. A wide degree of creativity and latitude is expected. Typically reports to top management.
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