The most prominent tool of SAS – PROC SQL : EpochResearch Institute India Pvt Ltd. (SASAuthorised Training : Ahmedabad | Bangalore)
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| Clinical SAS interview question & answers |
No need to brief in detail for
you as the title itself suggests what I mean to say, So yes, you are thinking
absolutely precisely about the topic. If you go through the post, this post
will surely help you some or the other way for your interview based
preparation.
Many of you wonder before
appearing for an interview and get wedged before the interviewer when answering
the technical questions. Instead of getting jammed, go through these questions
and be self prepared thoroughly in order to crack your interview. I have listed
some of the questions below:
1.
Illustrate
regarding the phase of Clinical trials
Phase I - Testing of a drug for the
safety purpose
Phase II - After the testing the
experimental drug is conferred to number of people to check its
effectiveness
Phase III – It is given to large number
people to check it’s effectiveness along with that side effect to be checked and
monitored and to be compared to commonly used treatments
Phase IV – The last phase includes the studies
that include drug risk, benefits and advantages.
2.
Explain
the validation procedure?
Validation
procedure is used to check the output of the SAS program. When the output
generated by the validator matches to the output generated by the SAS
programmer, then the program is deemed as valid.
3.
How
to perform the validation of the listing having 400 pages?
This is not
possible manually. In order to validate, first convert the listing to data sets
using PROC RTF and then you can compare using PROC COMPARE.
4.
Per
day, how many tables can be created?
Creating tables
generally depends on the complexity of the tables. If there are similar type
tables, atmost 4-5 tables can be created in a day.
5.
How
to generate tables, listings and graphs?
We can generate
as follows:
Listings – PROC REPORT
Tables – PROC FREQ,
PROQ MEANS, PROQ TRANPOSE and PROQ REPORT
Graph – PROC GPLOT
etc
6.
As
per your experience, what PROC have you came across and used?
Procedures such
as proc report, proc format, proc sort, etc.
7.
Till
now which data sets have you came across?
You can ans for
the same that till now I have came across the data sets and worked with
laboratory, demographic, analysis, adverse events and other data sets.
8.
What are
the documents that you have to submit to FDA?
I have to submit
ISS and ISE documents.
9.
How your
experience with CDISC was and which version have you used?
I didn’t have
any chance to work with CDISC but still I helped my project manager and
statistician in CDISC. Version 3 was used.
10.
Describe
me something about SAS documentation?
Anything that we
type in program to make it easily readable and explicable is called as SAS documentation. It includes header, footer, title
etc.
So these were my some of the
questions that would guide you for your preparation. In my next discussion and
post, I‘ll come up with the next questions. You can comment for the same if you
have any more queries. You can also contact us for SAS training.
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