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Description of job position

  • Participating in the selecting of facilities for carrying out clinical trials.
  • Monitoring the progress of clinical trials, supervising compliance with the defined procedure by the investigators.
  • Responsibility for reviewing the accuracy and data processing.
  • Communicating with the regulatory bodies and other institutions.
  • Preparing documents for the National Institute for Drug Control (NIDC) and the European Commission (EC).
  • Submitting regular reports on the progress of studies.

Position Clinical Research Associate - Pharmaceutical Industry in the labour market

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Women representation in position

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