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Statistical Programmer II / SAS Programmer

Roles & Responsibilities

  • Proficiency in SAS (Base, Macro, and Graph)
  • Sound knowledge of CDISC standards (ADaM, SDTM)
  • Proven clinical/statistical programming experience within pharmaceutical clinical development (CRO/Pharma) with at least 3 years of experience
  • Strong analytical and communication skills

Requirements:

  • Develop and validate SAS programs for datasets, tables, listings, and figures
  • Collaborate with global teams to support clinical trial analysis
  • Ensure compliance with CDISC standards and regulatory requirements
  • Support the electronic submission preparation and review

Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel is hiring for Statistical Programmer II and Senior Statistical Programmer roles as part of our growing Functional Service Provider (FSP) team.

💡 What you’ll do:

  • Develop and validate SAS programs for datasets, tables, listings, and figures
  • Collaborate with global teams to support clinical trial analysis
  • Ensure compliance with CDISC standards and regulatory requirements
  • Support the electronic submission preparation and review.
  • Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements.
  • Contribute to life-changing research in a flexible, remote-friendly environment

💻 What you’ll bring:

  • Proficiency in SAS (Base, Macro, and Graph)
  • Sound knowledge of CDISC standards (ADaM, SDTM)
  • Proven clinical / statistical programming experience within pharmaceutical clinical development (CRO/Pharma) - Minimum 3years experience is essential
  • Strong analytical and communication skills

🌱 What we offer:

  • Career growth and mentorship
  • Fully remote work options
  • A culture of integrity, respect, and innovation

Whether you're advancing your career or bringing senior-level expertise, Parexel empowers you to make a meaningful impact.

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