Clinical Trials Regulatory Specialist

UNLV; Las Vegas (NV); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Retirement plans

Tuition discounts

Job summary

UNLV is seeking a Clinical Trials Regulatory Coordinator in the Research Department, Kirk Kerkorian School of Medicine. The role focuses on preparing, submitting, maintaining, and overseeing regulatory documents for clinical studies, ensuring compliance with GCP, FDA regulations, and sponsor requirements.

You will act as the primary regulatory liaison with investigators, IRB, sponsors, and agencies.

Qualifications

• Minimum two years of experience in clinical regulatory research including grants or clinical protocols.
• Bachelor’s Degree from an accredited college or university.
• This position does not provide visa sponsorship.

Responsibilities

• Prepare, submit, maintain, and oversee regulatory documents for clinical research in compliance with federal, institutional, and sponsor requirements.
• Serve as primary regulatory liaison between investigators, IRB, study sponsors, and regulatory agencies.
• Ensure trials are conducted according to GCP, FDA regulations, and institutional standards.
• Perform regulatory activities under supervision of the Director of the Office of Clinical Trials and the Associate Dean of Research.

Education

Bachelor’s Degree

Job description

UNLV is seeking a Clinical Trials Regulatory Coordinator in the Research Department, Kirk Kerkorian School of Medicine. The role focuses on preparing, submitting, maintaining, and overseeing regulatory documents for clinical studies, ensuring compliance with GCP, FDA regulations, and sponsor requirements.

You will act as the primary regulatory liaison with investigators, IRB, sponsors, and agencies.