Biostatistician

Job Activities

* Based on the protocol, CRF, existing final study report, and high-level description of additional desired analyses, prepare detailed TLG and derived variable specifications in order for the analyses to be implemented by our statistical programming group.

* Performs detailed QC of TLGs and derived datasets programmed by our statistical programming group, including possible double-programming of key variables or tables

* Programs ad hoc or exploratory analyses (Tables, Graphs, Exploratory modeling) in SAS or S-Plus in order to explore areas where more formal analyses could be useful. * Performs QC of final documents, presentation slides, or e-submission deliverables (dataset specifications, data tipsheets) to ensure that results and methods are clearly and correctly presented

Skills

Required Qualifications

* Ph.D. in statistics/biostatistics with at least 1 years of clinical trials experience (industry or CRO) or Masters' degree in statistics/biostatistics with at least 3 years of clinical trials experience

* Effective English-language verbal and written communication skills * Substantial SAS programming experience * Substantial experience in preparing detailed analysis specifications Desirable Qualifications * Experience with regulatory submissions * Experience with oncology clinical studies

* Experience programming in S-Plus * Strong background in survival analysis method
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