Utah Licensed Regulatory Affairs Specialist

A company is looking for a Regulatory Affairs Specialist. Key Responsibilities Serve as the regulatory lead for assigned projects, providing strategic input throughout study planning, execution, and reporting Prepare and ensure the accuracy and completeness of regulatory documents and submissions Stay current with evolving regulatory requirements and provide recommendations in response to emerging issues Required Qualifications Bachelor's degree (or equivalency) with 4-8 years of directly related work experience, or a master's degree (or equivalency) with 2-6 years of experience Experience in regulatory affairs within a regulatory agency or the pharmaceutical, biotechnology, or CRO industry Knowledge of ICH, GCP, FDA, and international regulatory guidelines Demonstrated experience interacting with regulatory authorities, including the FDA Advanced degree (MS, PharmD, PhD, MD) is preferred

Created: 2026-03-05