
The Regulatory Associate role supports oncology clinical trials at UNC LCCC by ensuring strict adherence to federal regulations and Good Clinical Practice. Key responsibilities include preparing and submitting regulatory applications to the IRB and various committees, drafting informed consent forms, and managing compliance tracking for assigned disease groups. The position also involves preparing for audits, maintaining electronic regulatory binders, and contributing to process improvements through standard operating procedures and team mentoring. This opportunity appeals to candidates seeking to advance their expertise in clinical research compliance within a mission-driven environment focused on patient safety and research integrity. The role requires occasional evening or weekend availability and offers a collaborative setting for professional growth in a specialized oncology research department.



















