Clinical Development and Quality Manager

We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world. Proclinical is seeking a Clinical Development Quality Manager to join our client\’s team in Surrey. In this role, you will focus on ensuring compliance and mitigating risks related to clinical studies, adhering to Good Clinical Practice (GCP) and other relevant guidelines. You will lead internal audits and support regulatory inspections, maintaining a robust quality system. Develop and maintain a quality management system for clinical development activities. Coordinate audits of clinical sites, CROs, manufacturers, suppliers, and laboratories. Drive the creation and implementation of SOPs to support clinical trial processes. Prepare and review documentation for regulatory submissions. Provide training across all phases of clinical drug development. Collaborate with project teams to ensure compliance with ICH guidance and regulations. Report quality updates to senior management and stay informed on regulatory trends. Experience in GCP QA and knowledge of GMP. Proven track record in building and maintaining a Quality Management System. Effective communication and influence management skills. By submitting this application, you confirm that you\’ve read and understood our privacy policy, which informs you how we process and safeguard your data –