SAS
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SAS Clinical Programmer Details
Typical SAS Clinical Programmer duties and responsibilities include:
Job Description: You will be responsible for the preparation of M&S analysis
datasets, assisting in the preparation of M&S reports, performing quality control
on analysis datasets and M&S reports, and for the procedures necessary to enable
the electronic submission of M&S datasets and reports..
Responsibilities:
-
Analysis dataset preparation will require you to interact with members of drug development
teams to identify appropriate source data in pharmacokinetic and clinical databases
- Extract and merge this data using SQL and SAS programming to
create M&S analysis datasets in SAS transport file format.
- Assisting in the preparation of M&S reports will include preparation of tables, listings, and plots to be included in the report
- Management of the report review process to ensure that comments
are received and addressed in a timely manner.
- You will also be responsible for performing quality control
on the analysis datasets and report, and assisting M&S scientists in performing
quality
Qualifications:
-
Bachelors or Masters Degree in statistics,
science or engineering (including computer science).
-
Minimum 3-4 years experience in SAS
programming related to clinical drug development, as well as SQL, S-PLUS, and NONMEM
software.
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Familiarity with principles of quality
control and the testing and validation of computer program code.