Job Description
A leading clinical research organization in New Jersey is seeking an experienced Statistical Programmer to lead the development and validation of CDISC-compliant datasets for CNS clinical trials. The ideal candidate will have over 5 years of experience in statistical programming within the pharmaceutical or CRO industry, advanced proficiency in SAS, and strong communication skills. This role offers a contract position with a fully remote work environment. #J-18808-Ljbffr
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