Job Description

Job Description

Job Description

Be Part of a Dynamic Biostatistics & Biometrics Team

This global biopharmaceutical company is dedicated to advancing therapies for serious and rare diseases. The Biometrics team plays a key role in driving data integrity and analytical excellence across clinical development programs. The group fosters a collaborative and innovation-driven culture where data programming expertise directly contributes to regulatory success and clinical insights.

What's In Store For You

This is a full-time, contract-based opportunity located in Bridgewater, NJ. The role offers exposure to cutting-edge statistical programming initiatives and the chance to collaborate with highly skilled biostatisticians and data scientists supporting high-impact clinical studies.

How You Will Make An Impact

• Provide programming support for clinical trials and submission deliverables.
• Develop and maintain SDTM and ADaM datasets compliant with CDISC standards.
• Produce tables, figures, and listings for clinical studies and publications.
• Collaborate cross-functionally with Biometrics and Biostatistics teams.
• Build and maintain robust SAS macros and utilities to optimize workflows.
• Ensure quality, consistency, and efficiency in all programming deliverables.

Are You an Experienced SAS Programming Professional Ready to Make an Impact?

• Bachelor’s degree in Mathematics, Statistics, Computer Science, or related field.
• 5+ years of experience in SAS programming within the pharmaceutical or biotech industry.
• Strong expertise in CDISC standards (SDTM and ADaM).
• Experience supporting data for regulatory submissions.
• Familiarity with additional programming tools such as R, Python, or VBA is an asset.
• Strong attention to detail, communication, and organizational skills.

#dice

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