Senior Regulatory Coordinator - Complex Trials (Hybrid)

University Of Nebraska Medical Center; Omaha (NE); Hybrid; USD 60,000 - 85,000; Full time

Job summary

University of Nebraska Medical Center in Omaha, NE seeks a Regulatory Coordinator II to oversee all regulatory documents for complex studies in the CTO, ensuring IRB and committee requirements are met and timelines stay on track.

You'll communicate with investigators and study staff, supporting higher complexity trials such as Phase I or investigator-initiated studies, and help manage increasing workload with attention to accuracy and compliance.

Qualifications

• Bachelor's degree or equivalent
• Business Administration, Healthcare, Scientific or related field
• (Will consider seven years related education/experience)
• Experience in healthcare, science or clinical research administration

Responsibilities

• Oversee regulatory documents for complex studies in the CTO and ensure IRB compliance
• Communicate with investigators and study staff to ensure timely, compliant submissions and updates

Skills

Strong organizational skills

Verbal and written communication

Independent problem-solving

Education

Bachelor's degree or equivalent

Business Administration, Healthcare, Scientific or related field

Tools

Microsoft Excel

Microsoft Word

Microsoft PowerPoint

Microsoft Outlook

Job description

University of Nebraska Medical Center in Omaha, NE seeks a Regulatory Coordinator II to oversee all regulatory documents for complex studies in the CTO, ensuring IRB and committee requirements are met and timelines stay on track.

You'll communicate with investigators and study staff, supporting higher complexity trials such as Phase I or investigator-initiated studies, and help manage increasing workload with attention to accuracy and compliance.