Qualifications
Required:
• Clinical research experience, with in depth knowledge of clinical oncology as it pertains to clinical trials and studies.
• Demonstrated organizational skills to efficiently and effectively provide data management/monitoring support for multiple clinical trials and projects, providing accurate information in a timely manner.
• Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, etc.
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