Texas Licensed Regulatory Affairs Coordinator

Job Summary

A company is looking for a Regulatory Affairs Coordinator.

Key Responsibilities

• Manage regulatory processes and prepare protocol documents for clinical trials
• Communicate with central operations to resolve regulatory issues and maintain compliance
• Assist in the preparation of informed consent documents and monitor serious adverse events

Required Qualifications

• High school diploma or equivalent required; some college coursework preferred
• Minimum one year of experience in clinical research regulatory affairs or oncology required
• Associate's degree in a clinical or scientific discipline preferred for level 2 and senior positions
• Minimum three years of experience in clinical research or regulatory affairs required for level 2
• Minimum seven years of experience in clinical research or regulatory affairs required for senior level