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As a Senior Biostatistician, you will design, analyze, and interpret clinical trials, ensuring the quality of statistical deliverables and collaborating with cross-functional teams.

As a Senior Statistical Programmer, you will develop and validate SAS programs for clinical trial data analyses, support regulatory submissions, and lead studies, impacting patient health globally.

As a Principal Statistical Programmer, you'll oversee programming activities across studies, ensure quality and compliance, mentor junior team members, and collaborate with various departments on complex clinical trials.

Manage clinical trial budgets and contracts, ensuring timely execution and efficiency in study start-up processes while improving service delivery methodologies.

The Proposal Manager is responsible for managing the full proposal lifecycle, leading cross-functional teams, and ensuring deliverables meet client requirements in a dynamic environment.