Clinical Research Associate

130 467 zł (PLN)/yr

62,72 zł (PLN)/hr

2 909 zł (PLN)/yr

The average clinical research associate gross salary in Poland is 130 467 zł or an equivalent hourly rate of 63 zł. In addition, they earn an average bonus of 2 909 zł. Salary estimates based on salary survey data collected directly from employers and anonymous employees in Poland. An entry level clinical research associate (1-3 years of experience) earns an average salary of 93 466 zł. On the other end, a senior level clinical research associate (8+ years of experience) earns an average salary of 161 043 zł.

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190 566 zł (PLN)

46 %

Based on our compensation data, the estimated salary potential for Clinical Research Associate will increase 46 % over 5 years.

This chart displays the highest level of education for:
Clinical Research Associate, the majority at 100% with bachelors.

Typical Field of Study: Community Organization and Advocacy

See how education can impact your salary

Poland

Cost of living is calculated based on accumulating the cost of food, transportation, health services, rent, utilities, taxes, and miscellaneous.

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Poland (Polish: Polska [ˈpɔlska] ), officially the Republic of Poland, is a country in Central Europe. It extends from the Baltic Sea in the north to the Sudetes and Carpathian Mountains in the south, while its longest river is the Vistula. Poland has a temperate transitional climate and is the fifth-most populous member state of the European Union, with its sixteen voivodeships having a total population of over 38 million and covering a combined area of 312,696 km2 (120,733 sq mi). It is bordered...

Sourced from Wikipedia
Designs, administers, researches, and studies designated clinical trials including investigator selection (who is responsible for the conduct of the trial at the trial site), analysis of potential patient recruitment, and preparation of trial related documentation, following company standard operating procedures and in accordance with Good Clinical Practice. Establishes, monitors throughout its duration, and closes down trial sites on completion of... the trial. Coordinates with the ethics committee, which safeguards the rights, safety, and wellbeing of all trial subjects; and organizes ethics committee submissions with follow through to ensure successful outcome. Identifies and assesses the suitability of facilities to be used as the investigational/clinical trial site; sets up trial sites, which includes ensuring each center has the required trial materials, including the trial drug often known as the investigational medicinal product. Read More

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Disclaimer

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Professionals should subscribe to SalaryExpert’s Assessor Platform.

ERI’s compensation data are based on salary surveys conducted and researched by ERI. Cost of labor data in the Assessor Series are based on actual housing sales data from commercially available sources, plus rental rates, gasoline prices, consumables, medical care premium costs, property taxes, effective income tax rates, etc.

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