Clinical Trial Manager

As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will assume responsibility for an individual project, or many projects and communicate in an optimal way, making sure that specific client objectives are met. Responsible for the set-up and maintenance of the project(s). Partially responsible for the development of research protocols and documents, such as CRF, publications and clinical reports. Responsible for the management of the study budget. Establish and manage the study time-lines and protocol specific SOPs. Ensuring that the many different tasks during clinical development and marketing are achieved. The role involves selection of research sites and focuses completely on the product development programme and trials. ICON offers a range of additional benefits designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Benefits examples include various annual leave entitlements, health insurance, retirement planning, Global Employee Assistance Programme, life assurance, as well as flexible country-specific optional benefits.