Clinical Research Associate

666.343 kr. (DKK)/yr

320,36 kr. (DKK)/hr

14.859 kr. (DKK)/yr

The average clinical research associate gross salary in Denmark is 666.343 kr. or an equivalent hourly rate of 320 kr.. In addition, they earn an average bonus of 14.859 kr.. Salary estimates based on salary survey data collected directly from employers and anonymous employees in Denmark. An entry level clinical research associate (1-3 years of experience) earns an average salary of 476.814 kr.. On the other end, a senior level clinical research associate (8+ years of experience) earns an average salary of 821.556 kr..

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736.274 kr. (DKK)

10 %

Based on our compensation data, the estimated salary potential for Clinical Research Associate will increase 10 % 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

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Denmark

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

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Denmark (Danish: Danmark, pronounced [ˈtænmɑk] ) is a Nordic country in the south-central portion of Northern Europe. It is the metropolitan part of and the most populous constituent of the Kingdom of Denmark, a constitutionally unitary state that includes the autonomous territories of the Faroe Islands and Greenland in the North Atlantic Ocean. Metropolitan Denmark is the southernmost of the Scandinavian countries, lying south-west and south of Sweden, south of Norway, and north of Germany, with...

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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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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