We are currently seeking a Principal Auditor Quality Assurance to join our diverse and dynamic team. As a Principal Auditor Quality Assurance at ICON, you will play a pivotal role in ensuring the quality and compliance of clinical trials, interpreting regulatory requirements, and contributing to the advancement of inNvative treatments and therapies. **What you will be doing** + Leading and conducting comprehensive audits of clinical trial processes, systems, and documentation to ensure compliance with regulatory standards and guidelines. + Collaborating with cross-functional teams to identify areas for improvement in quality assurance processes and practices. + Developing and implementing audit plans and strategies to assess the effectiveness of quality management systems. + Providing expert guidance and recommendations to stakeholders on quality assurance best practices and regulatory requirements. + Contributing to the continuous improvement of quality assurance programs and initiatives. **Your profile** + Bachelor's degree in Life Sciences, Pharmacy, or related field; advanced degree preferred. + Minimum of 7 years of experience in quality assurance within the pharmaceutical, biotechNlogy, or CRO industry, with at least 3 years in a leadership role. + In-depth kNwledge of regulatory requirements and guidelines governing clinical trials (e.g., ICH-GCP, FDA regulations). + Strong analytical and problem-solving skills, with the ability to identify and address complex quality issues. + Excellent communication and interpersonal skills, with the ability to effectively interact with internal and external stakeholders at all levels.