Regulatory Lead, Clinical Trials

University of Nevada, Las Vegas; United States; On-site; USD 70,000 - 110,000; Full time

Benefits offered by this job

Health insurance

Paid time off

Retirement plans

Tuition discounts

Wellness programs

Onboarding program

Job summary

The University of Nevada, Las Vegas invites applications for the Clinical Trials Regulatory Coordinator in the Kirk Kerkorian School of Medicine. The role focuses on preparation, submission, maintenance, and oversight of regulatory documents for clinical studies, ensuring GCP, FDA, and institutional standards are met.

As the primary regulatory liaison between investigators, the IRB, sponsors, and agencies, you will interpret regulations, manage workflows, and support study teams under the

Qualifications

• Bachelor’s degree is required; 2–4 years of clinical regulatory experience preferred.
• Experience with regulatory submissions and document maintenance.
• Ability to collaborate with investigators, IRB, sponsors, and regulatory agencies.

Responsibilities

• Prepare, submit, and maintain regulatory documents for clinical studies.
• Oversee regulatory compliance to GCP, FDA regulations, and institutional policies.
• Act as primary regulatory liaison between investigators, IRB, sponsors, and agencies.

Skills

Regulatory coordination

GCP knowledge

FDA regs

IRB liaison

Education

Bachelor's degree

Job description

The University of Nevada, Las Vegas invites applications for the Clinical Trials Regulatory Coordinator in the Kirk Kerkorian School of Medicine. The role focuses on preparation, submission, maintenance, and oversight of regulatory documents for clinical studies, ensuring GCP, FDA, and institutional standards are met.

As the primary regulatory liaison between investigators, the IRB, sponsors, and agencies, you will interpret regulations, manage workflows, and support study teams under the