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office-based Clinical Research Associate - Czechia  

PSI (company)


Posted on : 17 January 2017

Project Description

  • University degree in Life Sciences, pharmacy, MD or RN 
  • Prior CRA experience with full scope of monitoring responsibilities; independent monitoring experience in the Czech Republic 
  • Hands-on knowledge of ICH GCP 
  • Good English skills 
  • Proficiency in standard MS Office applications 
  • Desire and ability to travel 
  • Excellent communication, planning and organizational skills 

  • Setup, coordination, monitoring and general administration of international clinical studies of novel medicinal products 
  • Conduct and reporting of all types of monitoring visits to clinical sites 
  • Communication with clinical investigators, vendors, and support services in regards to study progress 
  • Maintenance of appropriate documentation regarding clinical site management 
  • Participation in feasibility research 
  • Quality control, preparation for and attendance at company’s audits 
  • Training of investigators and clinical trial team members 

We offer 

  • Excellent working conditions in our office in Prague 
  • Friendly team of clinical research professionals worldwide 
  • Competitive salary and benefits package 
  • Personal and professional growth; access to training opportunities