The University of Kansas Medical Center Cancer Center is seeking a Regulatory Coordinator to manage study-specific regulatory and safety reporting across multiple clinical trials. You will ensure compliance with CFR, GCP, HIPAA and organizational policies.
Responsibilities include preparing and submitting documents to the IRB, maintaining the trial master file and study credentials, and supporting monitoring visits and audits.
#J-18808-LjbffrRegulatory Coordinator Cancer Trials (Hybrid: Remote) in workfromhome at Unknown Company
This position is listed as full time and onsite.