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Responsible for cross functional participation in study design, clinical protocol development, statistical methodology and modeling, sample size estimations, endpoint specification, study logistics, randomization plans, interim analyses, and statistical analysis plans.
May be the statistical member of Data Safety Monitoring Committee to ...
About the Role
The Associate Director of Biostatistics provides leadership and guidance as the statistical expert on project teams or within a therapeutic area. He/she is accountable for all statistical aspects of assigned clinical studies including trial design, protocol development, analysis and interpretation of results for publications and submissions. Assurance of scientific validity and quality deliverables according to requirements of international regulatory agencies. The Associate Director may mentor junior statisticians, interns or contractor statisticians and will report to the Director of Biostatistics.
What you'll do:
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