Clinical Research Statistician Leader

Há 3 dias


Lisboa, Lisboa, Portugal MAI Fortrea Development Limited Tempo inteiro
Job Overview

MAI Fortrea Development Limited is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. Our company provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.

We are conducting operations in more than 90 countries, transforming drug and device development for partners and patients across the globe.

About the Job

$120,000 - $150,000 per year, depending on experience.

Senior Biostatistician

A highly skilled Senior Biostatistician is required to join our exceptional team and contribute to groundbreaking research. 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.

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.
Requirements:
  • Minimum of 5 years 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.
Why Join Us:
  • Pioneering Research: Contribute to the forefront of clinical trials within multiple therapeutic areas.
  • Global Reach: Collaborate with researchers and experts from around the world, contributing to global innovation and scientific breakthroughs.
  • Career Growth: Expand your skill set and broaden your expertise in a supportive environment, with numerous opportunities for career advancement.
  • Impactful Work: Directly contribute 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.
  • Be Yourself: Inclusive and diverse working environment that values and appreciates individual contributions.
  • Life-Style: Flexibility to work remotely from anywhere, promoting a healthy work-life balance.
  • Together We Thrive: Access to a supportive network of professionals, fostering collaboration and continuous learning.


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