Please send suitable profiles along with rate and contact info.
Position Title: Clinical Stats Programmer
Location: Livingston, NJ Experience: 3 + Yrs
Duration: 6+ months
Our client, a leading pharmaceutical company, is looking for two Contract
SAS Programmer. They need statistical Programmer who will provide high
quality work in support of our clinical studies.
Evaluate programming tasks needed for clinical studies or
Assist Bio statisticians in design and setup of mock summary tables,
listings, and figures pertaining to safety and other parameters as
Create or modify SAS programs to generate the appropriate tables, listings,
and figures involved in the aforementioned activities and to prepare
documentation of all programs written. Assist in the design of specific or
integrated SAS databases.
Participate in the design and writing of global standard SAS programs.
Coordinate and guide the programming activities of on-site program
consultants and/or off site CROs; audit work as required.
You will have a coordinated work schedule to fit project requirements and
time lines while at the same time working independently with minimal
Bachelor's degree in Biostatistics, Statistics, Computer Science.
Three to five (3-5) years of
pharmaceutical industry experience in SAS programming.
Experience in data analytic concepts, logically analyze programming
Position Title: *SAS Programmer*
Location: Cambridge, MA
Duration: 6+ months(Long Term)
*The Statistical Programmer will be responsible for:*
- Writing and testing SAS programs from instructions provided by
Biostatisticians and Statistical Programmers to create tables, figures, and
listings reporting the results of clinical trials for investigational
- Performing quality control checks of SAS code and output
- Compliance with FDA/ICH/GCP regulations
- Application of good working knowledge of medical data, the design and
phases of clinical trials, statistics, relevant GCP/ICH/FDA regulatory
requirements, and the pharmaceutical industry to the execution of all tasks
Qualified Candidates should posses:
- B.S. in Biostatistics, Statistics, Computer Science, or a related field
- A minimum of 5 years of SAS and relevant pharmaceutical industry
- Experience with writing SAS programs from instructions
- Experience with all SAS language, procedures, and options commonly used in
clinical trial reporting
- Experience working with all types of safety data and coding dictionaries
(MedDRA and WHODRL)
*Thanks & Regards,***
1001 Durham Ave, Suite 200,
South Plainfield, NJ 07080
*Voice: 732-767-0700 *3003*
Fax No - 732-767-9669
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