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Senior Clinical Research Associate Princeton United States, Frankfurt Germany, Bengaluru India,  

ECRON ACUNOVA (company)


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
  • 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 

Locations

Princeton NJ 08540 USA60528 Frankfurt GermanyWhitefield Bangalore India

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