Regulatory Affairs Specialist I-III - Remote

Overview

The University of Arkansas for Medical Sciences is seeking a Regulatory Affairs Specialist to ensure compliance and administrative excellence for multiple clinical trials, contributing to the success of cancer research.

In Short

• Join the Winthrop P. Rockefeller Cancer Institute.
• Manage regulatory compliance for clinical trials.
• Collaborate with investigators and sponsors.
• Ensure adherence to federal regulations and quality standards.
• Participate in the development of electronic infrastructure for trials.
• Monitor protocol status and advise on requirements.
• Assist in the preparation of research protocols.
• Maintain regulatory documents and binders.
• Provide exceptional customer service.
• Contribute to a collaborative healthcare organization.

Requirements

• Bachelor's Degree in relevant field or equivalent experience.
• Experience in clinical research and FDA Regulatory Affairs.
• Must obtain CRS certification within two years of hire.
• Knowledge of federal regulations governing clinical research.
• Strong organizational and project management skills.
• Excellent written and verbal communication abilities.
• Ability to manage multiple complex projects.
• Oncology experience preferred.
• Relevant certifications (RAC, CCRP, CCRC) are a plus.

Benefits

• Health, dental, and vision plans available.
• Holiday, vacation, and sick leave.
• Education discount for staff and dependents.
• Retirement plan with up to 10% matching contribution.
• Career training and educational opportunities.
• Merchant discounts.
• Concierge prescription delivery service.