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Senior Biostatistician - FSP

Fortrea
paid time off, flex time, 401(k)
United States, North Carolina, Durham
Mar 03, 2026

Fortrea is looking for Senior Biostatisticians to join our sponsor dedicated team

As a Senior Biostatistician at Fortrea, you will play a crucial role in the design, analysis, and interpretation of clinical trials, directly impacting the development of innovative therapies and treatments. Supported by a diverse team of research professionals, you will collaborate closely with study teams, medical experts, and project managers to ensure the highest quality scientific research and statistical analysis.

Your Responsibilities:

  • Design and implement statistical strategies for clinical trials within various therapeutic areas.

  • Develop statistical analysis plans, ensuring their appropriateness for study objectives.

  • Perform statistical programming tasks using SAS for analyses and generate study reports.

  • Collaborate with cross-functional study teams to contribute statistical expertise and guidance.

  • Provide expertise on statistical methodology, sample size calculations, and innovative trial design.

  • Ensure the quality and integrity of statistical deliverables.

  • Oversight of all the statistical queries on multiple projects.

Your experience and qualifications:

  • Minimum of 5 years (Senior)of experience as a Biostatistician within a CRO, biotech or pharmaceutical company.

  • Solid understanding of statistical methods commonly used in clinical trials, including advanced concepts.

  • Extensive knowledge of CDISC standards.

  • Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs

  • Proven professional experience with SDTMs, ADaM datasets and TFLs

  • Strong knowledge of regulatory guidelines (e.g., FDA, EMA) and industry standards.

  • Excellent communication skills, with the ability to effectively collaborate and present complex data to non-technical audiences.

  • Advanced degree (Ph.D. or Master's) in Biostatistics, Statistics, or a related field.

  • Demonstrated ability to work independently, utilize problem-solving skills, and make sound decisions.

What you can expect from us:

  • Pioneering Research: Join a CRO at the forefront of clinical trials within multiple therapeutic areas.

  • Career Growth: Expand your skill set and broaden your expertise in a supportive and environment, with numerous opportunities for career advancement.

  • Impactful Work: Contribute directly to the development of groundbreaking therapies and treatments, improving the lives of patients worldwide.

  • Competitive Compensation: We offer a competitive salary package, comprehensive benefits, and a rewarding bonus structure.

  • Life-Style: Flexibility to work remotely from anywhere, promoting a healthy work-life balance.

You can be 100% home-based in US or Canada.

Pay Range: $120,000 - $150,000

Canada pay range: 110,000 - 140,000

Benefits: All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), and Company bonus where applicable. For more detailed information, please click here.

Application deadline: March 15, 2026

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Learn more about our EEO & Accommodations request here.

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