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Clinical Research Associate - United States, Germany, India  



Posted on : 10 April 2017

Project Description

Roles and Responsibilities
  • To maintain awareness of local regulatory  requirements, and to conduct studies in accordance with SOPs, guidelines and  ICH Good Clinical Practice guidelines 
  • Conduct as well as pre-/Post-processing of pre-study-,  initiation-, monitoring- and close out-visits 
  • Creating study relevant documents 
  • Communication with investigational sites Participation in  national/international project and investigational meetings 

  • Experience as a CRA 
  • Study of natural science (biology, chemistry),  medicine, pharmacy or qualification as medical documentalist, health care  specialist, paramedic professional  
  • Willingness to travel extensively 
  • The ability of a good  communication, dedication, reliability and a talent for organizing are required