Provide Statistical leadership to oncology clinical trials: developing trial design options and providing high quality decision support; Statistical lead for a specific oncology molecule/indication in Health Authority interactions and maintain an accountability thread to Biostatistics function TA leaders; Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management colleagues to meet project deliverables and timelines for statistical data analysis and reporting
Requirements:
10 years + (Bachelors); 8+ years (Masters); 2+ years (PhD): 0+ years (MD) of statistical analysis experience in the pharmaceutical or biotechnology industry (or at a CRO); Industry experience in the statistical analysis of biomedical data using statistical software; Extensive hands-on experience in oncology drug development including design and analysis of oncology trials and active participation in regulatory interaction
Text:
Associate Director, Biostatistics - Oncology Provide Statistical leadership to oncology clinical trials: developing trial design options and providing high quality decision support; Statistical lead for a specific oncology molecule/indication in Health Authority interactions and maintain an accountability thread to Biostatistics function TA leaders; Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management colleagues to meet project deliverables and timelines for statistical data analysis and reporting 10 years + (Bachelors); 8+ years (Masters); 2+ years (PhD): 0+ years (MD) of statistical analysis experience in the pharmaceutical or biotechnology industry (or at a CRO); Industry experience in the statistical analysis of biomedical data using statistical software; Extensive hands-on experience in oncology drug development including design and analysis of oncology trials and active participation in regulatory interaction
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