Design and conduct ad hoc analyses using data from oncology studies with minimal supervision
Guide contract research organizations and internal teams in preparing analysis files and performing statistical analyses
Review publications and assist with post-market study protocols and statistical analysis plans
Required Qualifications
MS or PhD in statistics or biostatistics with at least 5 years of pharmaceutical experience
2-3 years of oncology experience, preferably from Phases 2 to Phase IV
Strong knowledge of statistical methodologies and drug development trends
Excellent programming skills in SAS and/or R
Significant knowledge of pharmacology, clinical research, and medical terminology
Average salary estimate
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