Lead Statistical Programmer - Clinical Trials & Submissions

A leading clinical research organization located in New Jersey seeks a skilled SAS Programmer to manage project delivery and statistical analysis outputs for clinical trials. Responsibilities include converting specifications into SAS code, developing and validating macros, and providing training and mentorship to team members. Ideal candidates will have expertise in SAS programming, a strong understanding of drug development processes, and excellent organizational skills for managing multiple projects.

This role is crucial for ensuring compliance with regulatory standards in clinical trials.
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