Principal Statistical Programmer — Clinical Trials (Contract)

Confidential; Malvern (Chester County); On-site; USD 90,000 - 120,000; Full time

Job summary

A leading biotechnology company in Malvern, PA is seeking a Principal Statistical Programmer. This role involves working closely with biostatistics teams to deliver high-quality programming support for clinical trials. The ideal candidate will have over 5 years of SAS programming experience and strong knowledge of CDISC standards. This position is office-based for 4 days a week and offers a competitive contract for 6+ months.

Qualifications

• 5+ years of SAS programming experience in a clinical trial environment.
• Strong working knowledge of CDISC standards.
• Experience leading programming for multiple studies preferred.

Responsibilities

• Develop and validate SDTM and ADaM datasets in compliance with CDISC standards.
• Create and review tables, listings, and figures (TLFs) for clinical trial reporting.
• Collaborate with CROs to ensure timely and accurate data delivery.

Skills

SAS programming

CDISC standards knowledge

Statistical analysis

Problem-solving

Communication

Organization

Education

BS/MS in Statistics, Computer Science, Mathematics, or Life Sciences

Tools

SAS (Base, Stat, Macro, Graph)

R

Python

Job description

A leading biotechnology company in Malvern, PA is seeking a Principal Statistical Programmer. This role involves working closely with biostatistics teams to deliver high-quality programming support for clinical trials. The ideal candidate will have over 5 years of SAS programming experience and strong knowledge of CDISC standards. This position is office-based for 4 days a week and offers a competitive contract for 6+ months.