Clinical Trials Regulatory Specialist

Kirk Kerkorian School of Medicine at UNLV; Las Vegas (NV); On-site; USD 70,000 - 95,000; Full time

Job summary

UNLV invites applications for the Clinical Trials Regulatory Coordinator in the Kirk Kerkorian School of Medicine. You will manage regulatory documents for clinical studies, ensuring compliance with GCP, FDA regulations, and institutional policies, acting as primary liaison among investigators, IRB, sponsors, and regulators.

Requirements include a Bachelor's degree and 2–4 years in clinical regulatory research; visa sponsorship is not provided.

Qualifications

• Bachelor's Degree from an accredited college or university and 2–4 years of experience in clinical regulatory research or related areas.
• Visa sponsorship is not provided; candidates must be legally authorized to work in the United States at time of hire.
• Minimum two years of experience in clinical regulatory research including grants or clinical protocols.
• Preferred: clinical trial regulatory experience including pre-study preparation, activation, maintenance, and close-out.

Responsibilities

• Prepare, submit, maintain, and oversee regulatory documents for clinical studies in compliance with federal regulations and sponsor requirements.
• Serve as the primary regulatory liaison between investigators, IRB, study sponsors, and regulatory agencies.
• Ensure trials are conducted in accordance with GCP, FDA regulations, and institutional standards.

Skills

Regulatory research

IRB liaison

GCP/FDA compliance

Education

Bachelor's degree

Job description

UNLV invites applications for the Clinical Trials Regulatory Coordinator in the Kirk Kerkorian School of Medicine. You will manage regulatory documents for clinical studies, ensuring compliance with GCP, FDA regulations, and institutional policies, acting as primary liaison among investigators, IRB, sponsors, and regulators.

Requirements include a Bachelor's degree and 2–4 years in clinical regulatory research; visa sponsorship is not provided.