The UNC Lineberger Comprehensive Cancer Center (LCCC) oversees and coordinates oncology clinical trial research for the UNC School of Medicine and UNC Cancer Care. The UNC Lineberger Oncology Clinical Protocol Office (CPO) is primarily responsible for organizing, managing, conducting, and supporting these trials. Working with the CPO Medical Director and the LCCC Associate Directors, the Assistant Director of Regulatory Affairs and Compliance oversees CPO regulatory operations, and reporting requirements for oncology clinical trials associated with the Cancer Center. The position also oversees the CPO training program to ensure the highest level of quality in the clinical research conducted at the Lineberger Comprehensive Cancer Center
Education and Experience:
Five (5) years experience in a research regulatory environment, preferably in an academic or clinical trials industry setting. Progressive management responsibilities including two (2) years supervisory experience
The University of North Carolina at Chapel Hill is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex, sexual orientation, or status as a protected veteran.
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