CRA INTERVIEW 2026 WITH ALL CORRECT & 100%
VERIFIED ANSWERS|LATEST UPDATE|ALREADY GRADED
A+
Why IQVIA ✔Correct Answer-IQVIA is the leader in healthcare intelligence and creates highly
customized approaches for tackling unique challenges. From what I've seen, IQVIA offers a plethora
opportunities for learning and growth. I believe that this will provide an environment that will allow
me to enhance my skills and experience.
What does ALCOA-C stand for? ✔Correct Answer-Accurate (data documented correctly), Legible
(easy to read), Contemporaneous (data recorded in real time), Original (not photocopies),
Attributable (data collected by the appropriate staff; should be clear who created records and when
they were created), Complete (nothing should be left blank or unanswered)
What is FDA 1572? ✔Correct Answer-This is an agreement signed by the PI noting that they will
provide specific information and that they will comply with FDA regulations related to study conduct
(drugs or biologics)
Lists PI, location of site or satellite site, laboratories involved and radiology locations involved, and
sub-I's
What is the most important part of the FDA 1572 ✔Correct Answer-The signature section as it
documents their commitment to follow pertinent FDA regulations.
What is an SAE? Provide an example. ✔Correct Answer-An unfavorable event that results in death,
hospitalization, prolonged hospitalization, birth defects, disability, ect.
Example: Cancer, heart attack, stroke, ect.
What are the contents of ICF? ✔Correct Answer-In the document:
1. What the trial is for and how it will run
2. The risks and potential benefits
3. Responsibilities and confidentiality
4. The voluntary nature and participation
5. Alternative treatments
Process:
1. Potential subject is seated in a quiet room
2. There is an exchange of information about the research
3. The subject is to read the entire for
4. Time should be allotted to for Q&A
5. The subject should sign the form
6. Site to provide a copy of the signed document
7. This process should be documented
8. This process should take place when new information develops, for example an update to the ICF
How do you handle a non-responsive/difficult CRC/PI ✔Correct Answer-If the CRC is non-
responsive, I would escalate this to the PI to ensure oversight; however, if the PI is also not
VERIFIED ANSWERS|LATEST UPDATE|ALREADY GRADED
A+
Why IQVIA ✔Correct Answer-IQVIA is the leader in healthcare intelligence and creates highly
customized approaches for tackling unique challenges. From what I've seen, IQVIA offers a plethora
opportunities for learning and growth. I believe that this will provide an environment that will allow
me to enhance my skills and experience.
What does ALCOA-C stand for? ✔Correct Answer-Accurate (data documented correctly), Legible
(easy to read), Contemporaneous (data recorded in real time), Original (not photocopies),
Attributable (data collected by the appropriate staff; should be clear who created records and when
they were created), Complete (nothing should be left blank or unanswered)
What is FDA 1572? ✔Correct Answer-This is an agreement signed by the PI noting that they will
provide specific information and that they will comply with FDA regulations related to study conduct
(drugs or biologics)
Lists PI, location of site or satellite site, laboratories involved and radiology locations involved, and
sub-I's
What is the most important part of the FDA 1572 ✔Correct Answer-The signature section as it
documents their commitment to follow pertinent FDA regulations.
What is an SAE? Provide an example. ✔Correct Answer-An unfavorable event that results in death,
hospitalization, prolonged hospitalization, birth defects, disability, ect.
Example: Cancer, heart attack, stroke, ect.
What are the contents of ICF? ✔Correct Answer-In the document:
1. What the trial is for and how it will run
2. The risks and potential benefits
3. Responsibilities and confidentiality
4. The voluntary nature and participation
5. Alternative treatments
Process:
1. Potential subject is seated in a quiet room
2. There is an exchange of information about the research
3. The subject is to read the entire for
4. Time should be allotted to for Q&A
5. The subject should sign the form
6. Site to provide a copy of the signed document
7. This process should be documented
8. This process should take place when new information develops, for example an update to the ICF
How do you handle a non-responsive/difficult CRC/PI ✔Correct Answer-If the CRC is non-
responsive, I would escalate this to the PI to ensure oversight; however, if the PI is also not
