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Clinical Trial Administrator I (PL) Warsaw Poland,  

KCR (company)

Posted on : 30 July 2017

Project Description

location: warsaw (office-based)

the duties associated with the role include:
  • responsibility for all administrative aspects of Clinical research studies, according to project-specific guidelines, standard operating procedures, gcp guidelines and local law.
  • University/college degree
  • good command of English
  • Teamwork ability
  • excellent organisation skills, patience, attention to detail
  • responsibility, self-reliance and self-discipline
  • eagerness to learn medical/Clinical research vocabulary and procedures
if you wish to apply, please submit your cv using the button below.


Warsaw, Poland

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