Senior Biostatistician - FSP

About the position 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.

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.

Requirements

• 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.

Benefits

• 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.
• 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.
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