Over 25 years of experience in the coordination and management of complex clinical trials work building and developing relationships with internal and external partners, including those in industry, to support the successful delivery of allocated research projects whilst ensuring compliance with current regulation. I have an excellent knowledge and understanding of the regulatory requirements governing clinical research, with current GCP certification, and for the need for quality management systems to ensure compliance. My experience working in cancer clinical trials has enabled me to obtain detailed understanding of the management and delivery of clinical research over multiple sites and my experience working in an innovative environment at Precision Medicine Scotland has given me insights into the regulatory complexities of working with emerging technologies including genomic data, complex healthcare data sets and AI tools.