What is a Clinical Trials Regulatory Coordinator
Prepares regulatory submissions, maintains IRB and sponsor documentation, and ensures compliance with trial regulations and reporting requirements.
Clinical Trials Regulatory Coordinator Core Duties
Prepare IRB Submissions And Amendments | Maintain Regulatory Binders And Sponsor Documentation | Manage Safety Reporting And Regulatory Correspondence | Support Audits And Inspections.
Clinical Trials Regulatory Coordinator Education Requirements
Certificate Or Bachelor Degree In Regulatory Affairs Or Clinical Research With Regulatory Training
Clinical Trials Regulatory Coordinator License and Accreditation Agency
RAPS | Employer Credential
Clinical Trials Regulatory Coordinator Program Length
3 to 24 Months
Clinical Trials Regulatory Coordinator Salary Min and Max
$45000 to $90000
Clinical Trials Regulatory Coordinator Work Settings
Academic Medical Centers | CROs | Pharma Companies | Research Sites
Clinical Trials Regulatory Coordinator Key Skills
IRB Submissions | Regulatory Documentation | Safety Reporting | Audit Support
Look for These Programs
Regulatory Coordinator Training At Universities | Professional Bodies