Associate Director, Biostatistics – Early Phase

in Statistics/Biostatistics, a minimum of 5 years (for Ph.D.) and 8 years (for M.S.) of experience in biotech/pharma industry as a statistician for clinical trials.

Hands-on experience in design and analysis of oncology trials is a must.

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This position is to serve as a study level statistician for oncology studies, and to coordinate activities with other functional groups to ensure timely deliverables.

Provide statistical expertise for design, analysis and reporting of clinical studies.

Collaborate with various functions on study design and planning, protocol development, statistical methodology and analysis.

Develop statistical analysis plans and analysis specifications.

Collaborate with statistical programming to ensure that analysis is conducted per statistical plan and specifications.

Collaborate with data management and clinical operations to ensure robust CRF and database development and quality data collection.