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Senior Clinical Research Associate - United States, Germany, India  



Posted on : 27 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