About this role
Clinical Regulatory Specialist at RadNet. Location: Anaheim, California, United States. Role: maintaining documentation, ensuring compliance, monitoring sites Requirements: BS/BA in life science (or 5+ years clinical research experience), 3+ years research experience, able to obtain ACRP or SoCRA certification within 1 year, strong medical record review, GCP/FDA knowledge, and excellent communication. Category: Research and Development (R&D) Seniority: Mid Level Certifications: acrp, socra, gcp Commitment: Full Time Workplace: Onsite Languages: English