About this role
Quality and Regulatory Associate at Summit Clinical Research Solutions. Location: Corpus Christi, Texas, United States. Role: auditing studies, ensuring compliance, preparing submissions Requirements: 2+ years regulatory/quality experience in clinical research preferred; bachelor’s in scientific field or equivalent; knowledge of GCP, HIPAA, CFR; proficiency with Microsoft Office and Clinical Research IO; CITI and GCP training required. Category: Research and Development (R&D) Seniority: Entry Level Tools: Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint, Clinical Research IO Commitment: Full Time Workplace: Onsite Languages: English