REGULATORY COORDINATOR

The LSU Cancer Center has an opening for a Regulatory Coordinator to work with the Cancer Center Clinical Trials Office (CC-CTO). The Regulatory Coordinator will be responsible for supervising all regulatory activities and processing and submitting all documentation related to the Institutional Review Board (IRB), Research Review Committee (RRC), Clinical Trials Research Center (CTRC), and pharmaceutical company regulatory mandates as required for NCI, industry-sponsored, and investigator-initiated protocols. The Regulatory Coordinator must also maintain credentialing for all Cancer Center, partner, and contracted affiliate site Investigators and Research Associates through the NCI and related cooperative groups. Duties include monitoring Cooperative Group/Pharmaceutical broadcasts for updates, maintaining electronic and paper files for dissemination, writing consents, facilitating and processing new protocols, completing and submitting adverse event forms, preparing regulatory records for all site audits, and other duties as assigned.The selected candidate must be organized, possess good decision making, problem solving, time management, and organization skills while maintaining attention to detail and flexibility in a high pressure environment as demands change.