Associate Director, Good Clinical Practice (GCP) Audit and Vendor Management

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. This position within R&D Quality, Associate Director, Good Clinical Practice (GCP) Audit and Vendor Management is a senior role responsible for leading the strategy, execution, and oversight of vendor management and GCP audit activities to ensure compliance with GCP regulations. This role ensures that clinical trials and all vendors adhere to internal quality standards, regulatory requirements, and contractual agreements, thereby supporting the integrity and success of clinical research. The position involves leadership, cross-functional collaboration, regulatory engagement, and continuous improvement initiatives to optimize vendor management, auditing, and clinical trial compliance. The position will play a critical role in safeguarding the integrity, safety, and quality of clinical research processes and data The role also includes leveraging Veeva Vault and other vendor management tools to ensure efficient oversight and documentation of vendor performance. Key Responsibilities: Audit Planning, Preparation, Conduct and Reporting: Operationalize approved audit plans and strategies for R&D GCP audits (External & Internal audits), considering relevant regulations