Auditor, RDQA Clinical Quality Audit - Remote

Role: Clinical Quality Assurance Auditor responsible for executing and managing the global clinical audit program to ensure compliance with regulations, standards, and AbbVie's policies. Responsibilities: plan, schedule, conduct and report on investigator site, process, system, and affiliate audits; review and track Corrective Action Plans; support GCP inspections; contribute to quality system development and continuous improvement initiatives; provide GCP compliance advice to partners; promote education on clinical regulations. Requirements: Bachelor's in science or health profession; 3-5 years in biopharma or regulatory authority; 3-5 years QA/Clinical Research experience; strong analytical, communication, and project management skills; familiarity with ICH-GCP, EU Clinical Trial Directive; ability to work independently and adapt to changing priorities. Preferred: global clinical audit experience, knowledge of international clinical trial regulations. High-Value: clinical audits in a regulated biopharma environment, GCP compliance, international travel readiness. WorkSetup: flexible, with willingness for international travel.