Graham holds a PhD in Neuropharmacology from the University of Edinburgh Medical School. His more than 30 years of industry experience includes clinical operations, project management, regulatory consulting and business development. Formerly VP, Clinical Development, Travecta Therapeutics, Graham has also held senior management roles in UK and Singapore with Parexel, ICON, Quintiles and Syneos. He has directly managed 20 Phase II/III clinical programs that successfully gained marketing approval through submission to the US FDA.
Susan is responsible for U.S. project and clinical operations, including project management, study startup, monitoring and site management services. With over 25 years in clinical research, she brings experience in all phases of clinical trials, multiple therapeutic areas including over 12 years in oncology, and key leadership roles in clinical operations and financial management. She has helped develop or improve services for multiple U.S. Contract Research and Site Management organizations, as well as a national oncology site network. Her work with global and cross-functional teams brings added value to the George Clinical team as the Global Head of Therapeutic Strategy, Oncology.
Dr. Hettiarachchi specializes in clinical trial operational strategy for recruitment, retention and successful trial delivery. An experienced clinical trial specialist, he has nearly three decades of clinical research experience in academic research, CROs, Pharma and biotech. He has managed many global clinical trials from start-up to CSR in various therapeutic areas, specializing in pivotal renal trials (IgAN, CKD, DKD, etc.) and in supporting operational teams in APAC and globally. He is exploring opportunities for clinical trials in new countries where there is high patient availability.
Gillian specializes in early phase clinical trial management and developing productive relationships with key opinion leaders. With more than 20 years of experience in the pharmaceutical industry and contract research organizations, she has worked in all phases of drug development and across multiple therapeutic areas. She is experienced in local and international quality and technical standards, project operations and medical affairs. She has a proven ability to develop strategies to support new business proposals in the early phase research arena.
