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Senior Programmer Analyst

Fortrea

Role overview

Qualifications

  • 5+ years of experience in Clinical Programming
  • Experience with clinical trial data and clinical research environments
  • Strong analytical, problem-solving, and stakeholder management skills
  • Fluency in English

Responsibilities

  • Lead the development and support of clinical technology solutions across global studies
  • Design, validate, and optimize complex SAS programs, datasets, edit checks, listings, and reconciliations
  • Create impactful visual analytics dashboards using Spotfire and Tableau
  • Drive automation, standardization, and process improvements that enhance quality and productivity

Key facts

Hard skills

Other skills

  • Analytical Thinking
  • Problem Solving

About the company

Fortrea logo

Fortrea

Contract Research Organizations (CRO)

We are creative thinkers with decades of clinical trial experience who drive innovative solutions powered by insights from data and technology. As we tackle challenges in today’s world, we know that we need to be nimble and agile. That’s why we work side-by-side with our partners to eliminate inefficiencies from the process so we can help them deliver life-changing therapies faster for patients, caregivers and healthcare providers worldwide.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

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Job description

Senior Clinical Programmer Analyst

📍 Remote | Mexico

Join Fortrea and work from anywhere in Mexico while contributing to global clinical trials that help bring life-changing therapies to patients worldwide.

We're seeking an experienced Senior Clinical Programming & Analytics Specialist to lead the development of innovative clinical data solutions leveraging SAS, Medidata Rave, Oracle Inform, Spotfire, and Tableau.

This role combines technical expertise, strategic problem-solving, and cross-functional collaboration to drive data quality, operational efficiency, and meaningful clinical insights.

What You'll Do

  • Lead the development and support of clinical technology solutions across global studies.
  • Design, validate, and optimize complex SAS programs, datasets, edit checks, listings, and reconciliations.
  • Create impactful visual analytics dashboards using Spotfire and Tableau.
  • Serve as a technical SME for EDC systems, clinical programming, and data solutions.
  • Drive automation, standardization, and process improvements that enhance quality and productivity.
  • Partner with global Data Management, Biostatistics, and Clinical Operations teams to deliver high-quality results.

What You'll Bring

  • 5+ years of experience in Clinical Programming, Data Management, SAS Programming, Spotfire, Tableau, or EDC systems.
  • Experience with clinical trial data and clinical research environments.
  • Strong analytical, problem-solving, and stakeholder management skills.
  • Ability to work independently within a global, collaborative environment.
  • Fluency in English.

Why Fortrea?


✅ Work on global clinical trials with leading pharmaceutical and biotechnology companies
✅ Exposure to cutting-edge clinical technologies and analytics platforms
✅ Opportunities for technical leadership, innovation, and career growth within a leading global CRO
✅ Collaborative, diverse, and purpose-driven culture

Ready to use data, technology, and analytics to accelerate clinical research? Join Fortrea and make an impact on a global scale while enjoying the flexibility of a remote role in Mexico.

Learn more about our EEO & Accommodations request here.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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