Temporary Clinical Regulatory Affairs Coordinator

University of California, Irvine • Irvine, CA

22h • $33 - $34

About The Position

This recruitment is for Temporary Regulatory Affairs Coordinator position through UCI's internal temporary staffing service.

Duties include, but are not limited to:
Ensure successful management of the regulatory aspects of each study conducted through UCI's Center for Clinical Research.
IRB review submissions and approval maintenance; initial, amendment, continuos review, and closure.
Maintain documents, files, and OnCore records.

Requirements

• 2-3 years experience in regulatory/IRB and/or clinical research.
• Ability to read, write, and follow written and oral instructions in English.

Responsibilities

• Ensure successful management of the regulatory aspects of each study conducted through UCI's Center for Clinical Research.
• IRB review submissions and approval maintenance; initial, amendment, continuos review, and closure.
• Maintain documents, files, and OnCore records.

Benefits

• medical insurance
• sick and vacation time
• retirement savings plans
• access to a number of discounts and perks

What This Job Offers

• Career Level: Entry Level
• Education Level: No Education Listed