About this role
Regulatory Coordinator - Research Administration at Kumc. Location: Kansas City, Kansas, United States. Role: preparing submissions, maintaining records, coordinating start-up Requirements: 4 years related experience (education may substitute); experience with clinical research regulations (CFR, GCP, HIPAA); Microsoft Office proficiency; responsible for IRB/ancillary submissions, regulatory records, and study start-up coordination. Category: Research and Development (R&D) Seniority: Mid Level Tools: Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint Certifications: ccrc, ccrp, gcp training Commitment: Full Time Workplace: Onsite Languages: Shona, English