Associate Clinical Research

R$113.329 (BRL)/yr

R$54,49 (BRL)/hr

R$2.527 (BRL)/yr

The average associate clinical research gross salary in Rio de Janeiro, Brazil is R$113.329 or an equivalent hourly rate of R$54. This is 5% higher (+R$4.884) than the average associate clinical research salary in Brazil. In addition, they earn an average bonus of R$2.527. Salary estimates based on salary survey data collected directly from employers and anonymous employees in Rio de Janeiro, Brazil. An entry level associate clinical research (1-3 years of experience) earns an average salary of R$81.802. On the other end, a senior level associate clinical research (8+ years of experience) earns an average salary of R$140.945.

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R$135.250 (BRL)

19 %

Based on our compensation data, the estimated salary potential for Associate Clinical Research will increase 19 % over 5 years.

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

Typical Field of Study: Community Organization and Advocacy

See how education can impact your salary

Rio de Janeiro, Brazil

The cost of living in Rio de Janeiro, Brazil is 33% more than the average cost of living in Brazil. Cost of living is calculated based on accumulating the cost of food, transportation, health services, rent, utilities, taxes, and miscellaneous.

View Cost of Living Page

Rio de Janeiro (Brazilian Portuguese: [ˈʁi.u d(ʒi) ʒɐˈne(j)ɾu] ), or simply Rio, is the capital of the state of Rio de Janeiro. It is the second-most-populous city in Brazil (after São Paulo) and the sixth-most-populous city in the Americas. Founded in 1565 by the Portuguese, the city was initially the seat of the Captaincy of Rio de Janeiro, a domain of the Portuguese Empire. In 1763, it became the capital of the State of Brazil, a state of the Portuguese Empire. In 1808, when the Portuguese Royal...

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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