Write the SAS a junior clinical programmer writes: read trial data into SAS Studio, build and clean variables in the DATA step, handle clinical dates, merge datasets by subject, query with PROC SQL, summarise with PROC FREQ and PROC MEANS, reuse code with macros, derive an SDTM domain and an ADaM subject-level dataset, and produce a demographics table. It is the programmer track that opens from clinical data management; it is not a statistics course and it does not make anyone a biostatistician.
What you will be able to answer
A study team hands you raw demographics and adverse-event extracts as CSV files and asks for a subject-level summary by treatment arm for the investigator meeting. What can you produce in SAS?
A reproducible SAS program that imports the raw files, converts character dates to SAS dates, derives age and flags, merges demographics with treatment assignment by subject, builds an SDTM-style DM dataset and an ADSL-style subject-level dataset with population flags, summarises counts, percentages, means and ranges by arm with PROC FREQ and PROC MEANS, and writes a formatted demographics table to RTF or PDF — with logs checked for warnings and notes, and without claiming validated, submission-ready datasets.
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Course outline
Concept 1
Concept 1 · Get started in SAS Studio: libraries and datasets
Concept 2
After: sas-studio-and-libraries
Most clinical derivations — age groups, flags, categories — are a few lines of DATA step logic.
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Concept 3
After: data-step-basics
Clinical data is full of dates stored as text — and SAS can't calculate with any of them until you convert them.
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Concept 4
After: data-step-basics
Demographics in one file, treatment in another — the merge is where subjects quietly go missing.
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Concept 5
After: merge-by-subject
If you already know SQL, PROC SQL lets you write it inside SAS — and many clinical programmers use both.
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Concept 6
After: data-step-basics
Nearly every clinical summary table is built from two procedures: one that counts and one that averages.
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Concept 7
After: proc-freq-means
When the same summary runs for twelve lab tests, a macro writes it once.
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Concept 8
After: sas-dates-and-formats, merge-by-subject
SDTM is just structure until someone writes the code that puts raw data into it — that's the clinical programmer.
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Concept 9
After: sdtm-dm-programming
SDTM records what was collected; ADSL records who counts in which analysis.
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Concept 10
After: adam-adsl, proc-freq-means
The demographics table opens the results of almost every clinical study report — and now you can build one.
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28 candidates did not meet the course criteria.
Designing statistical analysis plans for clinical trials and analyzing the resulting datasets. Exceptionally rare for Pharm.D graduates — the role is heavily skewed toward M.Sc/PhD Statistics or Biostatistics candidates, and deep statistical programming (SAS, R, Python) is mandatory. Listed honestly: high pay and remote-friendly, but a Pharm.D needs a statistics upgrade to compete.
8 mapped employers
Explore path →Making clinical-trial data accurate, secure, and analysis-ready: CRF review, query generation and resolution, data cleaning, and database lock. Freshers enter through large IT/BPO hiring drives (TCS, Cognizant, Accenture) and global CROs (IQVIA, ICON, Parexel) — no coding needed at entry. Honest caveat: your clinical training gives little edge here; B.Pharm, life-science, and IT graduates compete equally, and software/SQL skills matter more than therapeutics.
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