Sr SAS Programmer

Job ID: 08800
Location:   [Remote]
Employment Type: Contract
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Senior Statistical Programmer

Location: Remote preferred with candidates ideally located in the RTP, NC market or East Coast (EST)

About the Role

Our client is seeking a Senior Statistical Programmer to support a clinical development program with a targeted BLA submission timeline. This role will focus on statistical programming, clinical data review, regulatory support, and collaboration across clinical and data management teams.

Key Responsibilities

  • Create, validate, and document datasets, tables, listings, and figures for clinical trial studies.
  • Review SDTM and ADaM datasets and support eCRT package preparation.
  • Provide ad-hoc programming and analysis support for clinical development and post-marketing activities.
  • Develop SAS programs to support internal monitoring, analysis, and scientific publications.
  • Support statistical programming activities related to clinical study reports and outsourced trials.
  • Collaborate with data management teams to support clinical data review and customized reporting needs.
  • Maintain study documentation in compliance with SOPs and audit standards.
  • Communicate technical concepts and programming results to both technical and non-technical stakeholders.

Required Qualifications

  • Strong experience with SAS programming in a clinical research environment.
  • Experience supporting clinical trial data analysis and reporting.
  • Hands-on experience with CDISC standards, including SDTM and ADaM datasets.
  • Experience creating tables, listings, figures, and clinical datasets.
  • Experience supporting regulatory submissions and clinical study reporting.
  • Strong communication and collaboration skills.
  • Ability to manage multiple priorities and work independently.

Preferred Qualifications

  • Experience supporting BLA, NDA, or other regulatory submission activities.
  • Experience supporting medical affairs or scientific publication initiatives.
  • Familiarity with outsourced clinical trial programming support.
  • Experience working within pharmaceutical, biotech, or CRO environments.

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