Regulatory Affairs Coordinator

Job Summary

A company is looking for a Regulatory Affairs Coordinator II.

Key Responsibilities

• Facilitate initial new trial submission for SRC and IRB review
• Develop the Informed Consent document for clinical trial protocols
• Prepare and submit protocol amendments during the IRB review process

Required Qualifications

• BA/BS required
• Prior regulatory or clinical research experience with an academic medical center or industry is a plus
• Detail-oriented with the ability to manage multiple projects simultaneously
• Strong organizational skills