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As Associate Director of Biostatistics, you will lead statistical planning and reporting for clinical trials, ensuring compliance and integrity in methodologies. You'll serve as a biostatistical consultant, engage in regulatory meetings, support major projects, and oversee the database lock and unblinding processes, while guiding on statistical expertise and risk management.

Lead the technical aspects of statistical programming for clinical trial analysis using R. Responsibilities include developing and validating R packages, conducting statistical programming, collaborating with statisticians, and ensuring quality and accuracy of clinical data outputs. Requires strong knowledge in ADaM, SDTM, CDISC, and experience in pharmaceutical clinical development.

The Technical Account Manager maintains client relationships, addresses inquiries on healthcare databases, provides training, and coordinates internal responses to enhance customer satisfaction.