The post holder will be a subject matter expert in ICH GCP and wider clinical trial regulations. They will be responsible developing, revising and maintaining quality systems and Standard Operating Procedures to ensure that the Trust can evidence compliance in the conduct of research with national policies and standards. The post holder will provide professional leadership and management for the Trust wide research service, including the development of strategic frameworks which are robust, auditable and concur with acceptable best practice and national policy as it relates to the conduct of clinical research.The post holder will establish business processes and procedures that satisfy the Trust’s statutory research obligations. You will provide a combination of subject matter expertise and management skills to ensure high levels of service delivery and regulatory compliance.