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.
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Position Clinical Research Associate - Pharmaceutical Industry in the labour market
In the salary ranking,
the job position takes
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- Detailed breakdown of all monitored non-financial benefits provided*
- Financial benefit analysis* * available when regression model is used
