Clinical Research Associate (CRA) in Poland

Dokumeds is looking for highly motivated and proactive clinical research professionals willing to develop together with the company in position of Clinical Research Associate (CRA) in Poland.

Job Responsibilities:

  • Site administration and site monitoring responsibility for assigned clinical studies according to Dokumeds and Sponsor Standard Operating Procedures, legal requirements and ICH-GCP Guidelines
  • Conduct of country and site feasibility
  • Site initiation, routine monitoring and close-out visits
  • Preparation and submissions to Ethics Committees/ Regulatory Authorities
  • Assistance in site contract management


  • University degree in medicine, pharmacy, nursing or biology
  • Minimum 1-2 years of previous on-site monitoring experience in CRO or Pharma company
  • Previous experience in preparation and submissions to Ethics Committees/ Regulatory Authorities
  • Thorough knowledge of ICH-GCP guidelines including an understanding of local regulatory requirements
  • Excellent knowledge of Polish and English languages
  • Availability to travel
  • Computer literacy
  • Driving license
  • Strong organizational, communication and teamwork skills

We offer:

  • Challenging job in a highly qualified team
  • Employee-friendly work environment
  • Competitive salary
  • Professional growth in Clinical Research field

Working time: Full-time work

Contact person: Luminita Neferu, Deputy of HR Manager

More Information (external link)

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