Texas Licensed Regulatory Affairs Coordinator

Job Summary

A company is looking for a Remote Research Regulatory Affairs Coordinator II.

Key Responsibilities

• Manages regulatory processes and prepares protocol documents for clinical trials
• Communicates with central operations to resolve regulatory issues and maintains compliance with SOPs
• Assists with quality improvement measures and prepares necessary documentation for IRB submissions

Required Qualifications

• High School Diploma required; Associate's degree in a clinical or scientific-related discipline preferred
• Minimum of three (3) years of experience in clinical research, regulatory affairs, or oncology-related field required
• Experience in Microsoft Office
• Experience working with Sponsor Monitor representatives preferred
• Experience in clinical research or regulatory affairs is preferred