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Title:Statistical Programmer
Salary:Open
Experience:5-10
Location:NC - RTP

Description:

This position provides programming support for the analysis of pharmacokinetic, clinical, and laboratory data and for the production of statistical summary tables, graphs, and listings.

Responsibilities:

·         Provides support for the production of integrated summaries of safety (ISS) and efficacy (ISE) which may include pooling of datasets as well as report generation, and preparation of files for eNDA.

·         Provides support for the review of clinical databases.

·         Represents Biostatistics and Statistical Programming (BSP) department at the clinical study level.

Requirements:

·         BA/BS in a scientific, mathematical, or computer-related discipline.

·         (5- 10) years of direct SAS programming experience in clinical research and/or the pharmaceutical industry. Some of that experience must be related to an NDA submission.

·         Must have a high level of SAS programming expertise and ability to use advanced SAS programming techniques, including macro language.

·         Knowledge of basic statistical procedures, tabular programming methods, as well as complex reporting procedures.

·         Knowledge of CDISC and ADaM requirements.

·         Experience with other statistical software (besides SAS) and UNIX environment a plus.

·         The ability to manage software implementation projects, XML expertise, and database knowledge including PL/SQL.

·         General systems administration and management skills are helpful but not required.

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