Research/Ag Specialist

University of Nebraska Medical Center • Omaha, NE

8d

About The Position

This position oversees regulatory documents for complex studies currently in the CTO. The specialist is responsible for understanding IRB and committee requirements and maintaining compliance with updates. The role also involves communicating with appropriate individuals to ensure timeliness and efficiency. It expands on the Regulatory Coordinator I position and focuses on higher-complexity clinical trials, including Phase I, transplant, CAR-T, and investigator-initiated trials, as well as an increasing workload and volume of studies.

Requirements

• 3 years of experience.

Responsibilities

• Oversee regulatory documents for complex studies in the CTO.
• Know IRB and committee requirements and maintain compliance with updates.
• Communicate with appropriate individuals to ensure timeliness and efficiency.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: No Education Listed