Senior Biostatistician - FSP

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,

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 .

Final date to receive applications:
March 15, 2026

#LI-ML1

Learn more about our EEO & Accommodations request here.

Required

Preferred

Job Industries

• Other