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Associate Director, Statistical Programming

Job

EPM Scientific

Remote

$180,000 Salary, Full-Time

Posted 1 week ago (Updated 3 days ago) • Actively hiring

Expires 8/3/2026

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Job Description

Associate Director, Statistical Programming EPM Scientific - 3.3 Philadelphia, PA Job Details $160,000 - $200,000 a year 1 day ago Qualifications SAS SAS language ICH guidelines Bachelor's degree Pharmaceutical company experience CDISC standards Vendor communication Cross-functional collaboration Data analysis software
Full Job Description Title:
Principal /
Associate Director, Statistical Programming Location:
King of Prussia, PA (Hybrid) I am currently partnered with a leading pharmaceutical organization seeking an Individual Contributor, Statistical Programmer to lead programming activities across multiple clinical development programs spanning the full drug development lifecycle. Key Responsibilities Lead and support statistical programming activities across multiple clinical studies and development programs. Develop, validate, review, and maintain SAS programs for data manipulation, analysis, reporting, and submission. Review external vendor deliverables (e.g., SDTM, ADaM, TLFs, Define.xml packages) to ensure accuracy, quality, and compliance with standards. Contribute to regulatory submissions, including NDA/BLA filings, integrated summaries (ISS/ISE), pooled analyses, and responses to health authorities. Qualifications Bachelor's degree in Statistics, Mathematics, etc. (Masters Preferred) 8+ years of statistical programming experience within the pharmaceutical or biotechnology industry. Strong proficiency in SAS programming Deep understanding of regulatory guidelines (ICH, GCP) and industry standards. Extensive experience with CDISC standards, including SDTM and ADaM Prior involvement in regulatory submissions (NDA/BLA) and associated deliverables (e.g., Define.xml, validation processes) preferred. Strong communication, organizational, and cross-functional collaboration skills. Solid knowledge of statistical methodologies applied to clinical trial data. Demonstrated experience working with or overseeing external CRO partners.