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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 

  • At least 5 years of experience as a CRA 
  • Team player with  strong communication and collaboration skills 
  • Ability to work with investigational sites
  • Excellent at planning, organizing 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