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Senior Clinical Research Associate - United States, Germany, India  

Company managed [?] Still accepting applications
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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 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