The purpose of this position is to independently coordinate and manage data entry for oncology treatment trials, perform site initiation activities, and facilitate the comprehensive compilation of research patient records according to federal regulations, Good Clinical Practice, and local and institutional policies. These responsibilities relate to the mission of the UNC / LCCC Protocol Office by maintaining the quality of research and by addressing patient safety and regulatory compliance which impact research quality and safeguard institutional integrity.
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Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed