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US-MD-Baltimore: Senior Biostatistical Programmer

Date: _04-Feb-2014_
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Senior Biostatistical Programmer

Responsible for the generation and validation of SAS programs for the analysis and transfer of clinical data from Phase I clinical trials. Supports projects in the generation of SAS output such as tables, listings, and figures to be included in Phase 1 Clinical Study Reports

-Produce analysis data sets, summary tables, data listings, and figures for clinical studies using SAS according to sponsor formatting specifications or as documented in the Statistical Analysis Plan. -QC/Validate SAS programs created by colleagues - Perform analysis of clinical data per defined requirements -Debug, troubleshoot, and review SAS programs -Other responsibilities as assigned by immediate supervisor -Map datasets according to sponsor specifications -Will work with our support staff and take the role as project lead -Responsible for mentoring more junior programmers Qualifications Experience -Some statistical training is desirable but not required -At least 2-5 years clinical and/or research experience preferred -Experience with Phase 1 clinical studies -Strong working knowledge of SAS (5 + years) -Strong analytical skills and ability to effectively apply technical knowledge to solve problems -Self-motivated, able to work independently, team player -Industry experience (Pharma or CRO) required

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