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SAS Programmer

Jersey City, NJ, United StatesPosted 124 months ago
ContractremoteMid-Senior Level

Job Description

If you are interested give me a call on 973-606-3290 or you can send me the copy of resume on himanshu.prajapat(at)collabera.com

Position summary: 

The role of the Senior Statistical Programmer is to perform statistical programming activities for all assigned Phase I-IV clinical studies. This position performs statistical programming for clinical studies, integrated summaries, and in support of responses to requests from regulatory authorities.

• Perform role of primary and validation statistical programmer on all assigned studies, integrated summaries, and in support of responses to questions from regulatory authorities.

• Create derived data set specifications for all assigned studies and integrated summaries.

• Create data definition tables for analysis data sets for all assigned studies and integrated summaries.

• Review statistical analysis plans for all assigned studies and integrated summaries and provide comments to study biostatistician.

• Review annotated case report forms and provide comments to study designer. 

• Represent Statistical Programming on all assigned project and study teams as needed




Position qualifications: 

• 3-5 years experience performing statistical programming with SAS in a pharmaceutical or CRO environment

• Bachelor’s Degree or above in Statistics, Biostatistics, Mathematics, Computer Science, or another related field.

To know more about this opportunity, please contact

Himanshu Prajapat

himanshu.prajapat(at)collabera.com

973-606-3290

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