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Senior Clinical Research Associate - United States, Germany, India  


Posted on : 10 April 2017

Project Description

Roles and Responsibilities Monitor clinical trials in accordance with SOPs, guidelines and ICH Good Clinical Practice guidelines. This will comprise performing pre-study-, initiation-, monitoring- and close out-visits. Communication with investigational sites to improve trail conduct and to strengthen motivation of site staff involved in EA projects Creating study relevant documents for submissions to competent authorities and ethics committees Be up to date with European and local regulatory requirements in clinical trials Participation in national and international project and investigational meetings Requirements At least 3 years of experience as a CRA Team player with strong communication and collaboration skills Ability to work with investigational sites in Germany Excellent at planning, organising and executing trial activities Ability to prioritize tasks, while keeping attention to important details Study of natural science (biology, medicine, pharmacy or nursing) or equivalent Willingness to travel Location Frankfurt


Princeton NJ 08540 USA 60528 Frankfurt Germany Whitefield Bangalore India

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