Regulatory Coordinator, Clinical Research Administration
Kumc
The University of Kansas Medical Center is seeking a Regulatory Coordinator in the RI Office of Clinical Trials Administration to manage study-wide regulatory and safety reporting across multiple protocols. You will ensure compliance with CFR, GCP, HIPAA and KU policies while serving as the primary contact for IRB submissions and maintenance of regulatory records. Responsibilities include preparing regulatory documents, tracking submissions, maintaining the trial master file, coordinating with #J-18808-Ljbffr Kumc
Vacancy posted 4 days ago
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