Clinical Research Associate -GSK-USA-Eugene, Oregon Portland, Oregon

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Working knowledge of GCPs and clinical trial processes
- Ability to manage multiple priorities across several protocols and therapeutic areas simultaneously
- Identify and recruit investigators, including sites new to GSK
- Conduct site initiation, monitoring and close-out visit activities
- Track study progress and submit subject data to GSK within specified timelines for assigned sites
- Actively contribute to the development of the U.S. Monitoring (USM) organization characterized by process standardization, best practice sharing and continuous improvement
- Work within a matrix environment, cultivating strong working relationships by partnering in a collaborative manner with all internal and external customers to achieve study goals
- Proactively contribute to the resolution of complex monitoring and regulatory issues through discussions with the appropriate internal departments (monitoring, compliance, study staff, etc.)
- Act as a resource for monitoring personnel regarding therapeutic and monitoring issues
- Contribute to the successful completion of special projects within the monitoring organization, as appropriate
- Take a lead role within USM by contributing as a monitor liaison and/or Lead CRA to clinical projects, as appropriate

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