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Clinical Trial Administrator I (PL) - 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.