Remote (Global) Full-time

Fortrea is hiring a Senior and Principal Biostatistician - FSP

About the Role

Fortrea is seeking Senior and Principal Biostatisticians to play a crucial role in the design, analysis, and interpretation of clinical trials. You will directly impact the development of innovative therapies and treatments, collaborating closely with study teams, medical experts, and project managers to ensure the highest quality scientific research.

What You'll Do

  • Design and implement statistical strategies for clinical trials across 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.
  • Oversee all the statistical queries on multiple projects.

What We're Looking For

  • A minimum of 5 years (for Senior) or 10 years (for Principal) 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.
  • An 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.

Technical Stack

  • SAS
  • SAS macros
  • SAS/STAT

Team & Environment

You will join a sponsor-dedicated team, collaborating with cross-functional study teams.

Benefits & Compensation

  • 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 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.

Work Mode

This is a remote position open to candidates in the EMEA region.

Fortrea is proud to be an Equal Opportunity Employer. As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.

Required Skills
SASSAS macrosSAS/STATStatistical AnalysisClinical TrialsCDISC StandardsProtocol DevelopmentStatistical ProgrammingRegulatory SubmissionsBiostatisticsData AnalysisStudy DesignStatistical MethodologyPharmaceutical Industry
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About company
Fortrea

A global CRO partner that supports mission-driven sponsors in bringing new therapies to patients.

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Posted 7 months ago