Principal Biostatistician
作为 Fortrea 的主要生物统计学员，你将在设计，分析和提供复杂的临床试验中发挥关键作用，支持从研究设计到监管提交等全球项目。在我们的全职服务团队内，你将与跨学科利益相关者合作，并提供战略统计领导力以确保高质量，有影响力的结果。你的责任：·负责复杂的研究和计划 （包括提交和多项协议工作）的统计策略和交付；·制定和审查统计分析计划，确保统计成果的质量 · 监督统计分析，表格，数字和列表 (TFL) 和研究报告 · 与跨职业团队密切合作并担任关键的统计顾问 · 支持监管互动，出版物和后期分析 · 参与研究设计，协议和随机化规划 · 导师年级统计人员并提供技术领导力 · 在客户互动，竞标防御和审计中代表生物统计学 • 经验和资格：· 高等学位 (MSc/PhD) 数据，生物统计或相关领域 · 具有重要的经验作为 CRO,生物统計或药品的主要生态技术专家 · 对于临床试验和监管要求的统计方法 (FDA/EMA) 的强知识 · SAS 方面的熟练知识 （包括先进程序）· CDISC 标准 (SDTM,ADaM,TFLs) 的实践经验 · 对各种利益相关者传达复杂的统计概念的能力 · 组织能力强大，细节关注和协作思维 · 英语流利：• 在复杂的，具有高影响力的全球研究工作 · 强大的职业发展和成长机会 ·竞争力补偿和全面收益 ·灵活，远程友好的工作环境 · 支持性，合作团队文化 福特雷亚正在积极寻找激励的解决问题和创造性思想家，他们分享我们克服临床试验障碍的热情。我们的坚定承诺是彻底改变开发过程，确保将改变生活的想法和治疗快速交付给需要患者。加入我们的卓越团队并拥抱一个协作工作空间，个人成长培养，使你能够产生有意义的全球影响。查看更多关于福特雷亞的信息。福特雷雅自豪地成为
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As a Principal Biostatistician at Fortrea, you will play a key role in the design, analysis, and delivery of complex clinical trials, supporting global programs from study design through to regulatory submissions and beyond.
Working within our Full Service team, you will partner with multidisciplinary stakeholders and provide strategic statistical leadership to ensure high‑quality, impactful outcomes.
Your responsibilities:
- Lead statistical strategy and delivery for complex studies and programs (including submissions and multi‑protocol work)
- Develop and review Statistical Analysis Plans and ensure quality of statistical outputs
- Provide oversight of statistical analyses, Tables, Figures & Listings (TFLs), and study reporting
- Collaborate closely with cross-functional teams and act as a key statistical advisor
- Support regulatory interactions, publications, and post hoc analyses
- Contribute to study design, protocols, and randomization planning
- Mentor junior statisticians and provide technical leadership
- Represent Biostatistics in client interactions, bid defenses, and audits
Your experience and qualifications:
- Advanced degree (MSc/PhD) in Statistics, Biostatistics, or related field
- Significant experience as a Lead/Principal Biostatistician in CRO, biotech, or pharma
- Strong knowledge of statistical methods for clinical trials and regulatory requirements (FDA/EMA)
- Proficiency in SAS (including advanced procedures)
- Solid experience with CDISC standards (SDTM, ADaM, TFLs)
- Ability to communicate complex statistical concepts to diverse stakeholders
- Strong organizational skills, attention to detail, and collaborative mindset
- Fluent in English
What you can expect from us:
- Work on complex, high‑impact global studies
- Strong career development and growth opportunities
- Competitive compensation and comprehensive benefits
- Flexible, remote-friendly working environment
- Supportive, collaborative team culture
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit .
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. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact:
. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.
Learn more about our EEO & Accommodations request here.
Originally posted on Himalayas