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

Try These Other Programs

Regulatory Coordinator Training At Universities | Professional Bodies