Posted to MedZilla on 12/25/2019


US-MD, Biostatistical/Senior Biostatistical Programmer


The Biostatistical/Senior Biostatistical Programmer is 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.

Key Accountabilities
-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

Job Posting Qualifications

-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
-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

Education – BS/MS in health related science or equivalent

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