Clinical Trials Regulatory Liaison

Nevada System of Higher Education; United States; On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Excellent health insurance (medical,-d

Tuition discounts at NSHE

Tuition discounts for spouses/partners

Wellness programming

Career advancement opportunities

Job summary

University of Nevada, Las Vegas invites applications for the Clinical Trials Regulatory Coordinator in the Research Department, Kirk Kerkorian School of Medicine. The coordinator oversees regulatory documentation for clinical studies, ensuring compliance with GCP, FDA regulations, and institutional policies.

The role serves as the primary liaison between investigators, IRB, sponsors, and regulatory agencies, supporting study activation, maintenance, and close-out in a fast-paced research

Qualifications

• Minimum two years of experience in clinical regulatory research, including grants or clinical protocols.
• Bachelor’s Degree from an accredited institution recognized by US DOE/CHEA.

Responsibilities

• Prepare, submit, maintain regulatory documents for clinical studies in accordance with federal regulations and institutional policies.
• Serve as primary regulatory liaison between investigators, IRB, study sponsors, and regulatory agencies.
• Ensure trials are conducted in compliance with Good Clinical Practice (GCP) and FDA regulations.

Skills

Regulatory coordination

IRB familiarity

Education

Bachelor’s Degree

Job description

University of Nevada, Las Vegas invites applications for the Clinical Trials Regulatory Coordinator in the Research Department, Kirk Kerkorian School of Medicine. The coordinator oversees regulatory documentation for clinical studies, ensuring compliance with GCP, FDA regulations, and institutional policies.

The role serves as the primary liaison between investigators, IRB, sponsors, and regulatory agencies, supporting study activation, maintenance, and close-out in a fast-paced research