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Clinical Research Associate

Question26: Please prepare an informed consent form for the imaginary drug Happymycin that would treat Mood Disorders (Depressions) ?

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Clinical Research Associate

Q25: Please prepare a draft of a CRF for the imaginary drug Happymycin that would treat Mood Disorders (Depressions).

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Clinical Research Associate

Question 24: Please prepare a draft of the IB for the imaginary drug Happymycin that would treat Mood Disorders (Depressions) . Please include all...

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Clinical Research Associate

Question23: Please write a draft of the protocol summary for the imaginary drug Happymycin that would treat Mood Disorders (Depressions). Please include all appropriate...

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Clinical Research Associate

Question22: What are general responsibilities of the sponsor in clinical trials according to ICH GCP?

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Clinical Research Associate

Question21 : What are general principles of the FDA guidance on the choice of control groups in clinical trials?

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Clinical Research Associate

Question20: What are general principles of the FDA guidance on the use of computerized systems in clinical trials?

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Clinical Research Associate

Question19: Please, list a CRA’s responsibilities in finalizing the study?

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Clinical Research Associate

Question18: Please list all of the important things to consider regarding volunteer recruitment. For example, you should consider advertisement, incentives, gender of candidates...

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Clinical Research Associate

Question17: What are some of the important points that should be considered during study Initiation?

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Clinical Research Associate

Question16: Please list what is to be expected of a CRA in relation to study monitoring?

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Clinical Research Associate

Question15: Please create a checklist for a pre-investigation visit for a phase II clinical trial on X-micine: a new anti-viral compound that reduces...

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