Clinical Research Associate (CRA) / Monitor (f/m/d) – Czech

  • Full time
  • Prague
  • Posted 1 week ago

based in Prague.

Your responsibilities:

  • Support of project management in terms of planning, organisation and implementation of national and international clinical studies of phases II to IV.
  • Conduct of monitor visits (initiation, monitoring of ongoing study activities and close-out) according to SOPs as well as applicable guidelines.
  • Support of and close cooperation with the trial sites as well as the corresponding departments of the sponsor.
  • Creation of study-relevant documents (e.g. for authorities and ethics committees) and project plans, selection of potential trial sites, preparation and implementation of training courses and presentations.


  • Have minimum 2 years of experience as CRA.
  • Are a natural scientist, medical doctor or have a corresponding qualification in the medical field.
  • Are a native speaker of Czech and have very good English language skills.
  • Are confident in the use of common MS Office programs.
  • Have knowledge of the ICH-GCP guidelines.
  • Are characterised by team-oriented and above all structured work, are reliable, communicative, flexible and enjoy travelling.


  • Ensure you a thorough introduction and support from a team of experienced natural scientists.
  • Offer exciting and varied projects from the pharmaceutical, biotech and medical production sectors.
  • Guarantee fast decision-making processes due to flat hierarchies and “open doors” culture.
  • Love diversity! Our teams are diverse, cross-generational and we work and learn with and from each other.
  • Have modern, well-equipped offices in the heart of Prague.
  • Provide you flexible home office options – during the pandemic and even afterwards.

Interested? The shortest way to join our team is via our application portal. We ask for applications in English.

To apply for this job please visit