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Job Title:SAS Programmer
Location:Atlanta, GA
Type: Full time
PROJECT DESCRIPTION:
A statistical programmer provides timely support to the study team on all
programming matters according to the project strategies. Requirements will
be identified according to a Statistical Analysis Plan and programming
specifications using internal standards and guidelines. Should have the
ability to generate all of the production tables needed for a given study,
and to work with other programmers and statisticians in providing a quality
review of the results. Must follow SOPs and department work instructions
with a minimum amount of supervision. Has the ability to work on multiple
projects and maintain timelines. Knowledge of SAS (Base, Macro, Stats)
required, and knowledge of the FDA is desirable, Production programming
experience is also a plus.
RESPONSIBILITIES:
- Oversees the ad hoc as well as production programming for three to four
clinical studies.
- Provides timely support to the study team on all programming matters
according to the project strategies.
- Requirements will be identified according to a Statistical Analysis Plan
and programming specifications using internal standards and guidelines
- Implements and executes the programming and project standards.
- Assists in the design and testing of program logic, coding programs,
program documentation and preparation of programs.
- Supports ongoing clinical studies requests for statistical and non-
statistical analyses. Provides documentation and consistent maintenance of
code, logs, and output in a regulated environment.
- Ability to support data cleaning effort, and to work with statisticians
and data managers.
- Ability to support study requirements with challenging timelines under
direct supervision of the Associate Director of Statistical Programming.
- Support team within a study team involved in the creation and QC of
production tables, figures, and listings (TFLs) in support of analysis
requirements utilizing Regeneron tools and methodologies.
- Follows department SOPs, and Work instructions as well as Server
requirements.
- Supports the marketing activities for the protocols supported.
- Assures that results included in presentation are consistent with results
in source /output prior to release.
EDUCATIONAL REQUIREMENTS:
- Bachelor’s or Master’s degree required
- 2-5 year’s experience as a Statistical Programmer
TECHNICAL SKILLS:
Clinical SAS Programmer responsible for creating tables, listings, figures
and analysis data sets. Consultant should have at least 3 years of clinical
SAS experience working in the Biostatistics department. Good understanding
of Analysis Data Sets and Procs. Experience with STDM, using CDISC, and/or
ADaM programming is a plus, but not required. SAS, S-Plus (or R), JMP, and
MS Office. Knowledge of FDA requirements is desirable. Ability to work in
fast-paced environment is required.
CORE COMPETENCIES:
- Must be able to work in a consistently busy environment.
- Flexibility and multi-tasking are highly desirable skills for this
position.
- Written and oral communication skills |
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