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Clinical Research Associate Prague Czechia,  

KCR (company)

Posted on : 08 March 2017

Project Description

The duties associated with the role include:
  • Performing site visits and monitoring activities in accordance with protocol, GCP/ICH Guidelines and other applicable requirements 
  • Ensuring overall integrity of study and adherence to guidelines, protocol and regulations 
  • Taking an active role in the project team by providing feedback and suggestions for successful completion of the project 
  • Coaching and mentoring less experienced CRAs to assist in their development and training  

  • University degree in life sciences/pharmacy/biotechnology 
  • At least 1 year of independent monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) according to protocol monitoring guidelines, SOPs, GCP/ICH Guidelines 
  • Computer competency 
  • Fluent command of English 
  • Ability to complete tasks in an accurate and timely manner        


Czech Republic Prague

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