Summary: The senior/principal biostatisticians will be supporting Phase 2 or 3 studies and be hands-on with data checking, programming, and statistical analysis deliverables under guidance.
Qualifications: Master's in Statistics, Biostatistics, or related field with 5+ years of experience in the design, analysis, and reporting of clinical studies. OR PhD in a related field with 3+ years of experience Demonstrated experience in SAS programming with a specific emphasis on SAS procedures used in programming statistical analyses commonly used in the analysis of clinical study data. Significant experience working with CDISC and related FDA standards for specification and creation of SDTM and ADaM datasets.

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Level

Senior L5

Location

Port Reading, NJ

Occupation

Biostatisticians

Industry

Research and Development in Biotechnology (except Nanobiotechnology)

Posted

2 days ago

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