Clinical Research Associate I/II

该职位来源于猎聘 Overview As a Clinical Research Associate (CRA) you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. You will be managing competing priorities, supporting the on-site team, ensuring investigators follow the clinical trial protocol, providing training, and most importantly, motivating the team to ensure high quality results. The Role and your ResponsibilitiesTo assist the study management teams in completion of all required tasksTo have thorough understanding of clinical trialsTo assist project teams with study specific documentation and guidelines as appropriateTo contribute to the creation of CTMS guidelines and provide training on themTo assist in co-ordination of investigator payments, if applicableTo co-ordinate document translation, if requiredTo assist with the coordination of team member tracking; What is Required Education (minimum/desirable):A degree in a scientific or health care discipline preferred. Languages: Fluent English (oral and written). Experience/Professional requirement:Solid medical and business knowledge. 2. at least 1 years CRA experience.Knowledge and experience in international (FDA, EMEA) and local regulations as well as Novartis standards.Good communication skillsAbility to manage multiple prioritiesComputer literacy.