Clinical Research Associate I Interview Questions
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Clinical Research Associate I interview questions shared by candidates
Clinical Research Associate I was asked...June 9, 2016
Why do you want to leave your current position and why? What makes you want to work at children? What regulatory experiences do you have? Have you worked with grading toxicities? How do you handle stress?
3 Answers↳
I want a relocat
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I want a relocat
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I want a relocat
Clinical Research Assistant I was asked...October 1, 2015
What is your plans?
2 Answers↳
To grow up in the field of the Clinical Research
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What other questions did they ask you?
Clinical Research Associate I was asked...September 12, 2022
What do you do if you have a deadline due and you don't have time?
1 Answers↳
Delegate, see if you can postpone, do it!
Clinical Research Assistant/Coordinator I was asked...November 15, 2016
Would I be able to commit longer than a year?
1 Answers↳
Yes I will be able to commit longer than a year
Clinical Research Associate I was asked...November 7, 2016
Q: What was one thing that they asked you? What improvements if any you would made regarding your working environment?
1 Answers↳
How did you answer this question? (Optional)
Clinical Research Coordinator I was asked...February 17, 2021
Standard public health questions to understand demography and willingness to learn new skills such as phlebotomy
1 Answers↳
Looking for jobs in clinical research in neighboring states
Clinical Research Coordinator I was asked...July 20, 2013
They brought in 3 doctors from the department and had each one talk about their research.
1 Answers↳
Be prepared to talk about/ask questions about their research
Senior Intern/Clinical Research Associate I was asked...October 21, 2014
Clinical Research Associate I was asked...August 9, 2016
Clinical Research Associate I was asked...March 28, 2016
In your own words, what is a CRA?
1 Answers↳
A CRA responsibility is to monitor the progress of the clinical trial and to ensure that the study is conducted and that data are handled in accordance with the protocols, good clinical practices, and all FDA and regulatory requirements. The CRA make sure that data are accurately verified and recorded in the electronic data capture system. Less